SCIENTIFIC PROGRAM
THURSDAY, AUGUST 31
12:00 – 17:00 Registration
17:00 – 17:30 Opening Ceremony
Welcome addresses
PLENARY SESSION 1:
Clinical Genetics and Cytogenetics
17:30 – 19:00
Chair persons: Prof. Thilo Dörk
Prof. Milena Stevanovic
17:30 – 17:50 PS01. Prof. Thilo Dörk – Hannover, Germany
The molecular and biochemical basis of chromosomal instability syndromes
17:50 – 18:10 PS02. Prof. Tayfun Ozcelik – Ankara, Turkey
X-chromosome inactivation and evolution: a statistical study of skewed X-chromosome inactivation in autoimmune diseases
18:10 – 18:30 PS03. Prof. Milena Stevanovic – Belgrade, Serbia
Fluorescent in situ hybridization (FISH): Our experience
18:30 – 18:50 PS04. Prof. Miroslava Micic – Belgrade, Serbia
Genetic Profile of Males Treated at Infertility Clinic in Belgrade
18:50 – 19:00 Discussion
19:00 Get together
FRIDAY, SEPTEMBER 1
PLENARY SESSION 2:
Cancer Genetics
08.30 – 09:40
Chairpersons: Prof. Kresimir Pavelic
Prof. Aleksandar Dimovski
8:30 – 8:50 PS05. Prof. Kresimir Pavelic – Zagreb, Croatia
Molecular Profiling of Tumors: from Benchside to Bedside
8:50 – 9:10 PS07. Prof. Aleksandar Dimovski, Josifovski T., Petrusevska N. – Skopje, R. Macedonia
Molecular Aspects of Colorectal Cancer Management
9:10 – 9:30 PS08. Dr. Natalia Bogdanova – Hannover, Germany
Latest advances in the identification of breast cancer susceptibility alleles
9:30 – 9:40 Discussion
PLENARY SESSION 3:
The Status of Molecular Genetics in Balkan Countries
9:40 – 11:10
Chairpersons: Prof. Ivo Kremensky
Prof. Marieta Costache
9:40 – 10:00 PS09. Prof. Georgi D. Efremov – Skopje, Republic of Macedonia
Molecular Genetics in Republic of Macedonia
10:00 – 10:20 PS10. Prof. Ivo Kremensky – Sofia, Bulgaria
Prevention of Inherited Disorders and Congenital Anomalies in Bulgaria
10:20 – 10:40 PS11. Dr. Marieta Costache – Bucharest, Romania
Approaches in Molecular Diagnostics of Cancer and Muscular Dystrophy in Romania
10:40 – 11:00 PS12. Dr. Veronica Karcagi – Budapest, Hungary
Muscular Dystrophies – Diagnostic Approaches in Hungary
11:00 – 11:10 Discussion
11:10 – 11:40 Coffee brake
PLENARY SESSION 4:
Prenatal Diagnosis and Therapy for Genetic Diseases
11:40 – 13:10
Chairpersons: Prof. Joep Geraedts
Prof. Akif Yesilipek
11:40 – 12:00 PS13. Prof. Joep Geraedts – Maastricht, The Netherlands
Preimplantation Genetic Diagnosis as an Alternative for Prenatal Diagnosis
12:00 – 12:20 PS14. Prof. Mehmet Akif Curuk – Adana, Turkey
Prenatal diagnosis of hemoglobinopathies in Turkey; prelude to preimplantation diagnosis for sickle cell anemia
12:20 – 12:40 PS15. Prof. Akif Yesilipek – Antalya, Turkey
Stem Cell Transplantation in Hemoglobinopathies
12:40 – 13:00 PS16. Prof. Grigor Zoraqi – Tirana, Albania
Human Artificial Chromosomes as Vectors in Gene Therapy
13:00 – 13:10 Discussion
13:10 – 15:00 Lunch
15:00 – 16:00 POSTER PRESENTATIONS (PP01-PP82)
Chairpersons: Prof. Mirko Spiroski
Prof. Mirjana Kocova
Dr. Veronica Karcagi
ORAL PRESENTATIONS – SESSION 1
Cancer Genetics
16:00 – 17:00
Chairpersons: Prof. Damjan Glavac
Dr. Natalia Bogdanova
16:00 – 16:10 OP01. Ravnik Glavac M., Berginc G., Potočnik U., Golouh R., Glavač D. - Ljubljana, Slovenia
Molecular genetic screening of microsatellite instable colorectal cancer and Lynch syndrome
16:10 – 16:20 OP02. Aveic S., Petrucev B., Dokmanovic L., Radmilovic M., Tosic N., Stojiljkovic M., Karan-Djurasevic T., Kostic T., Janic D., Pavlovic S. - Belgrade, Serbia
Optimization of therapy for thiopurine s-methyl-transferase deficient childhood acute lymphoblastic leukemia patients
16:20 – 16:30 OP03. Dimova I., Orsetti B., Rouge C., Ursule L., Lasorsa L., Dimitrov R., Doganov N., Toncheva D., Theillet Ch. - Sofia, Bulgaria
Genomic profiling of ovarian cancer for chromosome 17 by array CGH analysis
16:30 – 16:40 OP04. Eren P., Bozkurt S., Kılıç T., Turan K., Erdağ B., Sav A., Pamir M.N ., Çırakoğlu B - Istanbul, Turkey
Relations between EGFR, PTEN, PDGFR-α, MGMT expression patterns and TP53 and P53 pathway (MDM-2 and P14ARF) gene aberrations in low grade gliomas
16:40 – 16:50 OP05. Onrat T.S., Ellidokuz E., Küpelioğlu A., Durhan E. - Afyon, Turkey
P53 and APC gene mutation analyses in cases with colon cancer
16:50 – 17:00 Discussion
ORAL PRESENTATIONS – SESSION 2
Molecular Basis of Monogenic and Complex Diseases
17:00 -18:00
Chairpersons: Prof. Borut Peterlin
Prof. Nazli Basak
17:00 – 17:10 OP06. Jordanova A., Tourne v I., Guergueltcheva V., Litvinenko I., Ishpekova B., Bozinova V., Kremensky I. - Sofia, Bulgaria
Molecular genetics of inherited peripheral neuropathies in Bulgaria
17:10 – 17:20 OP07. Stevanovic A., Stojiljkovic M., Petrucev B., Tosic N., Karan Djurasevic T., Kostic T., Djordjevic M., Stojanov Lj., Pavlovic S. - Belgrade, Serbia
Phenylketonuria in Serbia and Montenegro
17:20 – 17:30 OP08. Kaneva R., Angelicheva D., Milanova V., Hallmayer J., Macgregor S., Alexiev S., Ivanova M., Vladimirova R., Stoyanova V., Milenska T., Kremensky I., Jablensky A., Kalaydjieva L. - Sofia, Bulgaria
Fine mapping analysis of bipolar affective disorder in Roma families
17:30 – 17:40 OP09. Arsov T., Farrell G., O'Bryan M., Sainsbury-Salis A., Goodnow C. - Garran, Australia
Genetic and phenotype analysis of fat aussie - a mouse model of Alström syndrome
17:40 – 17:50 OP10. Egorova O.V., Bermisheva M.A., Khusnutdinova E.K., Glebova N.N., Dodonov A.N. - Ufa, Russia
Association between uterine leiomyoma and estrogen metabolism and estrogen receptor genes polymorphisms in Russian population (Bashkortostan)
17:50 – 18:00 Discussion
SATURDAY, SEPTEMBER 2
PLENARY SESSION 5:
Genetic Epidemiology, Population Genetics & Diversity and Bioethics
08:30 – 10:40
Chairpersons: Prof. Elza Khusnutdinova
Prof. Alex Felice
08:30 – 08:50 PS18. Prof. Ingeborg Barisic, Dolk H, Eurocat Working Group – Zagreb, Croatia
Epidemiologic Surveillance of Congenital Anomalies in Europe
08:50 – 09:10 PS19. Prof. Elza Khusnutdinova, Bermisheva M., Kutuyev I., Khusainova R., Malyarchuk B., Stepanov V., Kivisild T., Villems R.– Ufa, Russia
Phylogeography of Y-chromosomal and mitochondrial lineages and language affinities of Eurasian populations
09:10 – 09:30 PS20. Prof. Alex Felice – Malta
Significance of Molecular Epidemiology in a Small Island Population
09:30 – 09:50 PS21. Dr. Damir Marjanovic – Saraevo, Bosnia and Herzegovina
Historical overview of human population-genetic studies in Bosnia and Herzegovina during the last three centuries
09:50 – 10:10 PS22. Prof. Mirko Spiroski – Skopje, Republic of Macedonia
Y-STR haplotypes in Republic of Macedonia
10:10 – 10:30 PS23. Prof. Helena Kaariainen – Turku, Finland
Genetic Counselling, Genetic Education and Bioethics
10:30 – 10:40 Discussion
10:40 – 11:10 Coffee break
PLENARY SESSION 6:
Molecular Basis of Monogenic and Complex Diseases
11:10 – 13:20
Chairpersons: Prof. Pier Franco Pignatti
Prof. Henry Wajcman
11:10 – 11:30 PS24. Prof. Pier Franco Pignatti - Verona, Italy
Ecogenetics and Pharmacogenetics of Coronary Atherosclerosis
11:30 – 11:50 PS25. Prof. Borut Peterlin – Ljubljana, Slovenia
Genomic Biomarkers for Neurodegenerative Disorders
11:50 – 12:10 PS26. Prof. Nazli Basak, Saner N. – Istanbul, Turkey
A Heterogeneous Group of Disorders: Spinocerebellar Ataxias
Genetic Bases and Molecular Diagnoses
12:10 – 12:30 PS27. Prof. Henri Wajcman, Baudin-Creuza V., Vasseur-Godbillon C., Marden M.– Creteil, France
Alpha Hemoglobin Stabilizing Protein and Hemoglobin Disorders
12:30 – 12:50 PS28. Prof. Damjan Glavac – Ljubljana, Slovenia
Molecular basis of Alport syndrome and benign familial hematuria
12:50 – 13:10 PS29. Prof. Mirjana Kocova – Skopje, Republic of Macedonia
Genetics of Congenital Adrenal Hyperplasia due to 21 Hydroxylase deficiency
13:10 – 13:20 Discussion
13:20 – 15:00 Lunch
15.00 – 16.00 POSTER PRESENTATIONS (PP83-PP183)
Chairpersons: Prof. Tayfun Ozcelik
Dr. Dijana Plaseska Karanfilska
Prof. Mehmet Akif Curuk
ORAL PRESENATATIONS - SESSION 3
Genetic epidemiology, Population Genetics & Diversity; Cytogenetics; Prenatal Diagnosis
16:00 – 17:00
Chairpersons: Prof. Ingeborg Barisic
Dr. Damir Marjanovic
16:00 – 16:10 OP12. Plaseska-Karanfilska D., Skopje, R. Macedonia
Partial AZFc deletions in Macedonian infertile males
16:10 – 16:20 OP14. Petlichkovski A., Efinska-Mladenovska O., Strezova A., Trajkov D., Arsov T., Spiroski M. - Skopje, Macedonia
Ambiguous allele combinations in HLA class II sequence-based typing in Macedonian population
16:20 – 16:30 OP15. Balikova I., Dimitrov B., Devriendt K., de Ravel T., Ganev V., Kalev I., Vermeesch R.J., Simeonov E. and Fryns J.P. - Sofia, Bulgaria
Molecular karyotyping - novel powerful tool for gene identification
16:30 – 16:40 OP16. Vazharova R., Milashich T., Petrova V., Azmanov D., Yosifova A., Becheva E., Kamenova R., Dimitrova V., Hranov Y., Koleva G., Velev R., Damjanova V., Toncheva D. - Sofia, Bulgaria
Cytogenetic and molecular - cytogenetic studies of spontaneous abortions
16:40 – 16:50 OP17. Andonova S., Raynova R., Kremensky I. - Sofia, Bulgaria
Rapid detection of selected aneuploidies with molecular methods - advantages and disadvantages
16:50 – 17:00 Discussio
ORAL PRESENATATIONS - SESSION 4
Clinical Genetics; Therapy for Genetic diseases; Genomics & Proteomics
17:00 – 18:00
Chairpersons: Prof. Miroslava Micic
Prof. Grigor Zoraqi
17:00 – 17:10 OP18. Dimitrov B., Vermeesch J.R., Hannes F., Balikova I., De Ravel T.J., Debeer P., Devriendt K., Fryns J-P. - Leuven, Belgium
Genetics of Trigonocephaly
17:10 – 17:20 OP19. Jurca C., Bembea M., Florea O., Bembea D. - Oradea, Romania
Retrospective study regarding the treatment in a series of 4311 patients with genetic disorders
17:20 – 17:30 OP20. Baran Y., Gündüz U., Senkal E.C., Bielawski J., Öğretmen B. - Ankara, Turkey
The involvement of ceramides in imatinib induced apoptosis and drug resistance
17:30 – 17:40 OP21. Mojsin M., Kovačević-Grujičić N., Krstić A., Stevanović M. - Belgrade, Serbia
Structural and functional characterization of the human SOX3 promoter
17:40 – 17:50 OP22. Petrovic I., Stevanovic M. - Belgrade, Serbia
Transcriptional regulation of human SOX18 gene - the role of SP1 transcription factor
17:50 – 18:00 Discussion
18:00 Concluding remarks
POSTER PRESENTATIONS
Posters should be placed on their specific numbered positions. The poster numbers can be found in the Scientific program – Poster presentations and in the Author index at the end of the Abstract Book (Proceeding of the 7th BMHG 2006). Poster mounting will be possible on Thursday, August 31 from 12:00-17:00 hours. Posters will be on display from Friday, September 1, 2006 (8:30 hours) to Saturday, September 2 (19:00 hours)
Dimensions: Posters should not exceed the maximum height x width of 120 x 100 cm
PP01. Yuce H., Tekedereli I., Ceylan G., Elyas H. - Elazig, Turkey
Cytogenetics in male infertility
PP02. Yüce H., Ceylan G., Etem E., Erol D., Özbey U., Deveci D., Kara M., Elyas H. - Elazig, Turkey
Screening of Yq polymorphisms in Turkish males
PP03. Cinar C., Yazici C., Ergünsu Ş., Beyazyürek Ç., Javadova D., Sağlam Y., Tarcan T., Güney İ. - Istanbul, Turkey
Genetic diagnosis in infertile men with numerical and constitutional sperm abnormalities
PP04. Yuce H., Ozbey U., Etem E., Erol D., Ceylan G., Deveci S., Kara M., Elyas H. - Elazig, Turkey
Cytogenetic and clinical evaluation of Klinefelter's Syndrome cases determined by Medical Biology and Genetic Department of Medical Faculty in Firat University in term of 2000-2006
PP05. Erol D., Ceylan G., Yuce H. - Elazig, Turkey
An azoospermic male with 46,x,+marY karyotype
PP06. Yuce H., Ozbey U. - Elazig, Turkey
A case with 46,x, +mar (y), inv(y) (p11.2 →p11.2) karyotype
PP07. Babameto – Laku A., Mokin V., Cikuli M., Mitre A. - Tirana, Albania
Balanced tranlocation 14q21q in a patient with Klinefelter syndrome
PP08. Milashich T., Vazharova R., Yosifova A., Dimova V., Chernev T., Dimitrova V., Hranov U., Krustev K., Toncheva D. - Sofia, Bulgaria
Frequency of chromosomal abnormalities among families with reproductive failure
PP09. Djurkovic J., Andjelic L., Knezevic M. - Subotica, Serbia
Cytogenetic analysis of miscarriages in pregnancy early stages
PP10. Yuce H., Tekedereli i., Elyas H. - Elazig, Turkey
Cytogenetic results of recurrent spontaneous abortions in Turkey
PP11. Etem E., Yüce H., Deveci S., - Elazig, Turkey
The case with primary amenorrhea presented with a 46,X,del(X),(q23)
PP12. Lazovska B., Popova M., Georgieva S. - Skopje, Macedonia
The frequency of chromosome abnormalities detected in girls with primary and secondary amenorrhoea
PP13. Sredovska A., Sukarova-Angelovska E., Kocova M. - Skopje R. Macedonia
Karyotype in girls with Turner syndrome who develop spontaneous puberty
PP14. Etem E., Yuce H. - Elazig, Turkey
A case of Ullrich-Turner syndrome with 45,X(%73.4) /46,XY (%27.7) karyotype developed gonadoblastoma
PP15. Pendina A. A., Efimova O.A., Leont'eva O.A., Fedorova I.D., Kuznetzova T.V. and Baranov V. S. - Saint-Petersburg, Russia
Stage-specific DNA methylation patterns of metaphase chromosomes in human preimplantation embryos
PP16. Babameto – Laku A., Cikuli M., Mokin V., Mitre A. - Tirana, Albania
Partial trisomy 13q3 syndrome due to de novo duplication
PP17. Vasilevska M., Anevska-Mitrevska A., Stefanovska A-M., Lazarevski S.
Balanced reciprocal translocation 46XX, t(3,5) in IVF patient: A case report
PP18. Bajic V, Potparevic-Spremo B., Djelic N., Zivkovic L. - Belgrade, Serbia
The genetics of premature centromere separation syndromes
PP19. Cirkovic S., Guc-Scekic M., Vujic D., Micic D - Belgrade, Serbia
Chromosome instability of children with bone marrow failure - single centre experience
PP20. Drakulic D., Seović M., Čuturilo G., Jovanović I., Stevanović M. - Belgrade, Serbia
Detection of 22q11.2 deletion syndrome by fluorescent in situ hybridization (FISH)
PP21. Etem E., Ozbey U., Yuce H. - Elazig, Turkey
Cytogenetic evaluation of ambiguous genitalia in pediatric patients
PP22. Gorovenko N.G., Yevseenkova E.G., Zerova – Lyubimova T.E., Sheiko L.P., Tishchenko N.A., Brishevac L.I. - Shupyk, Ukraine
The usefulness of FISH-method for diagnosis of Williams-Beuren syndrome
PP23. Iourov I.Y., Vorsanova S.G., Monakhov V.V., Soloviev I.V., Kurinnaya O.S., Yurov Y.B. - Moscow, Russia
The basic and practical implications of quantitative fluorescence in situ hybridization (QFISH)
PP24. Kirbiyik O., Ozkinay F., Ercal D., Akin H. - Izmir, Turkey
A fetus with bisatellited maternally inherited chromosome 15
PP25. Ozcan Caliskan M., Mıhci E., Berker Karaüzüm S., Tacoy S., Luleci G. - Antalya, Turkey
Cryptic subtelomeric chromosomal rearrangements in cases with idiopathic mental retardation and dysmorphic features
PP26. Onrat T.S., Tomatir A.G - Afyon, Turkey
Observing with FISH methods for shortening of telomere with essential hypertension
PP27. Ozbey U., Kara M., Yuce H. - Elazig, Turkey
Applications of cytogenetic and Molecular genetic testing in Individuals with mental retardation
PP28. Etem E., Ozbey U., Yuce H. - Elazig, Turkey
Molecular screening of Fragile X (FRAXA) and FRAXE mental retardation syndromes
PP29. Ozturk S., Satman I., Pehlivan D., Cefle K., Palanduz S., Duman N. - Istanbul, Turkey
Case: Prader-Willi syndrome
PP30. Seovic M., Drakulić D., Bocić M., Branković-Nikšić S., Stevanović M. - Belgrade, Serbia
Detection of Prader-Willi syndrome using Fluorescent in situ Hybridization
PP31. Tica V., Mihalcea A., Luca C., Costache M., Ionica E. - Bucharest, Romania
FISH analysis of 17q /Brca1 in colorectal cancer
PP32. Vorsanova S.G., Iourov I.Y., Voinova-Ulas V.Y., Gorbachevskaya N.L., Demidova I.A., Beresheva A.K., Monakhov V.V., Kravets V.S., Kolotii A.D., Yurov Y.B. - Moscow, Russia
Molecular cytogenetic study of low-level chromosomal mosaicism in children with autism by interphase FISH
PP33. Yurov Y., Iourov I.Y., Kolotii A.D., Beresheva A.K., Liehr T., Vorsanova S.G. - Moscow, Russia
Interphase FISH study of aneuploidy rate in the brain tissues of patients with Ataxia-telangiectasia
PP34. Usurelu D., Teleanu M-V., Cimponeriu D., Radu I., Gavrila L. – Bucharest, Romania
Micronucleus induction by doxorubicin
PP35. Guven G.S., Cuna T. Birinci N., Guven M., Onaran I., Hacihanefioglu S. Ulutin T. - Istanbul, Turkey
17-b estradiole induced micronucleus formation in human lymphocytes
PP36. Andreea Iren Serban, E. Condac, Anca Dinischiotu, Marieta Costache -
Bucharest, Romania
Effect of hight-glucose concentration on the expression of type I and III collagen in cultured human skin fibroblasts
PP37. Kadiyska T., Goranova T., Dineva G., Nedin D.G. , Alexandrova A.B., Gegova A., Kaneva R.P., Damyanov D.N., Mitev V.Iv., Kremensky I.M. - Sofia, Bulgaria
Genetic testing for hereditary nonpolyposis colorectal cancer in Bulgaria
PP38. Petrova D.T., Nedeva P., Maslyankov S., Toshev S., Yaramov N., Atanasova S., Toncheva D., Oellerich M., von Ahsen N. - Sofia, Bulgaria
Genotyping of 3435 C>T and 2677 G>T MDR1 polymorphisms in Bulgarian patients with colorectal cancer and controls, as well as in tumor and surrounding normal tissues
PP39. Toma M., Belusica L., Cimponeriu D., Apostol P., Stavarachi M., Dumitrescu I., Craciun A-M., Dana U., Radu I., Gavrila L. - Bucharest, Romania
Molecular analysis of mutations for the APC gene in Romanian patients with colorectal cancer
PP40. Mihalcea A., Tica V., Tesio C.D., Dinischiotu A., Costache M., Ionica E. Bucharest, Romania
Molecular markers significance in colorectal cancer
PP41. Onrat T.S., Ellidokuz E.,Küpelioğlu A., Durhan E. - Afyon, Turkey
APC gene mutation analyses in cases with colon cancer
PP42. Onrat T.S., Ellidokuz E., Küpelioğlu A., Durhan E. - Afyon, Turkey
P53 intronic variant G13964C analyses in cases with colon cancer
PP43. Onrat T.S., Ellidokuz E., Küpelioğlu A., Durhan E. - Afyon, Turkey
Gene mutation analyses of p53 Arg72Pro in cases with colon cancer
PP44. Sterjev Z., Serafimovska Z., Kapedanovska A., Hiljadnikova-Bajro M., Josifovski T., Panovski M., Suturkova L., Dimovski A.J. - Skopje, R. Macedonia
Low penetrance allels predisposing to colorectal cancer in Macedonian patients
PP45. Josifovski T., Hiljadnikova-Bajro M., Sterjev Z., Kapedanovska A., Serafimovska Z., Panovski M., Suturkova L., Dimovski A.J. - Skopje, R. Macedonia
Genomic instability patterns in patients with colorectal cancer from Macedonia
PP46. Josifovski T., Hiljadnikova-Bajro M., Sterjev Z., Kapedanovska A., Serafimovska Z., Panovski M., Suturkova L., Dimovski A.J. - Skopje, R. Macedonia
Familial colorectal cancer in Macedonia
PP47. Konstantinova D.V., Kadiyska T.T., Kaneva R.P., Ivanov S.I., Dimitrov R.G., Meinhardt K.P., Doganov N.I., Mitev V.I., Kremensky I.M. - Sofia, Bulgaria
Microsatelite instability in Bulgarian endometrial cancer patients
PP48. Kubelka Sabit K., Prodanova I., Yashar G., Zografski G., Basheska N. - Skopje, Macedonia
Prognostic significance of the HPV status in early stage cervical carcinoma
PP49. Nisevic I., Dinic J., Lukic S., Ugljesic M., Nikolic A. - Belgrade, Serbia
Analysis of MTHFR C677T mutation in patients with pancreatic cancer
PP50. Etem E., Bulut Y., Akpolat N., Korkmaz E., Yüce H., Yapar M. - Elazig, Turkey
Investigation the association between human herpesvirus (HSV) 1, 2, 6 , 7 positive and TLR9 gene polymorphism in the prostate cancer
PP51. Aral C., Çağlayan S., Massoumilary S., Sönmez O., Baloğlu H., Özışık G., Akkiprik M., Özata M., Özer A. - Istanbul, Turkey
Association of p53 codon 72 polymorphism with thyroid cancer in Turkish patients
PP52. Eren P., Uyar S., Topuzoğlu A., Kılıç T., Aker F., Erdağ B., Sav A., Pamir M.N., Çırakoğlu B - Istanbul, Turkey
Aberrations in TP53 and P53 pathway (MDM-2 and P14ARF) genes in low grade gliomas and their clinical effects
PP53. Eren P., Uyar S., Kılıç T., Topuzoğlu A., Erdağ B., Sav A, Pamir M.N , Çırakoğlu B - Istanbul, Turkey
Preferential localization of low grade gliomas with increased MGMT and P53 expression
PP54. Koynova D., Jordanova E., Kukutsch N., van der Velden P., Toncheva D., Gruis N. - Sofia, Bulgaria
Increased c-myc copy numbers on the background of CDKN2A loss is associated with improved survival in nodular melanoma
PP55. Koynova D., Tsenova V., Kunev K.,Toncheva D. - Sofia, Bulgaria
Analysis of separate and combinatorial aberrations of EGFR, C-MYC, ZNF217 and CCND1 genes in larynx cancer
PP56. Gucev Z., Koceva S., Muratovska O., Glamocanin S., Jovanov Gj., Vankovska V., Tasevska L., Taseva B., Jancevska A. - Skopje, Macedonia
BCR/ABL fusion in a child with chronic myeloic leucaemia
PP57. Lungeanu A., Arghir A., Berbec N., Chirieac S., Mocanu G., Angelescu S. - Bucharest, Romania
Complex chromosomal abnormalities identified in chronic myeloid leukemia at diagnosis
PP58. Berbec N., Chirieac S., Arghir A., Angelescu S., Lungeanu A. - Bucharest, Romania
Aberrant basophilia in chronic myeloid leukemia and additional chromosomal changes
PP59. Ilieva G., Cevreska L., Kocova M. - Skopje, R. Macedonia
Non specific chromosome deletion in M3 non-lymphocytic leukemia
PP60. Kokkinou S., Tzanidakis C., Lindou A., Alafaki H., Hatzikyriakou R., Floropoulou G., Haralambopoulou A., Fakiri E., Pavlou K. - Athens, Greece
Persistent polyclonal B-cell lymphocytosis: high-risk transformation to lymphoma. Cytogenetic and molecular study of 34 cases
PP61. Bagatir G., Palanduz S., Sirma S., Özbek U., Nalçaci M., Öztürk S., Çefle K., Candan S.
- İstanbul, Turkey
Is there any relation between the NQO1 C609T polimorphism and cytogenetics abnormalities in mds ?
PP62. Arghir A., Chirieac S., Berbec N., Vulcan G., Lungeanu A. - Bucharest, Romania
Myelodysplastic syndrome with numerical and structural chromosome abnormalities - case report
PP63. Luleci G., Doherty R., Lubinski J., Manguoglu E., Christie M., Bancroft E., Mitra A., Morgan S., Zieba K., Eeles R. - Antalya, Turkey
AIDIT and IMPACT: Strengthening research ties in Eastern Europe
- CLINICAL GENETICS AND DYSMORPHOLOGY
PP64. Cefle A., Cefle K., Ozturk S., Pehlivan D., Palanduz S. - Istanbul, Turkey
Klinefelter syndrome and systemic lupus erithmatohosus: case report
PP65. Papazovska-Cerepnalkovski A., Kocova M. - Skopje, R. Macedonia
Persistent Müllerian duct syndrome and association with Klinefelter's syndrome
PP66. Bembea M., Jurca C., Costea S., Bembea S., Jurca A., Harbuz R. - Oradea, Romania
Phenotypic variability in Dandy-Walker complex
PP67. Bembea M., Jurca C., Todor C., Skrypnyk C., Spineanu R., Iuhas O. - Oradea, Romania
Singular and syndromatic Ano-rectal malformations
PP68. Candan Ş., Tatlı B., Kara B., Kayserili H. - Istanbul, Turkey
Moebius syndrome with unilateral cerebellar hypoplasia
PP69. Durmaz B., Cogulu O., Dereli T., Ozkinay C., Ozkinay F. - Izmir, Turkey
A case of Kindler syndrome with primary infertility
PP70. Grkovic S. - Belgrade, Serbia
Pfeiffer syndrom: specificity of clinical features – possibility of prenatal diagnosis
PP71. Cefle K., Ozturk S., Tutkan G., Atar E., Palanduz S. - Sehremini Fatih, Turkey
Beckwith-Wiedemann Syndrome presenting with primary amenorrhea
PP72. Cinar A., Kuskucu M., Yilmaz S., Deviren A., Yüksel A., Hacıhanefioğlu S. - Istanbul, Turkey
A nonmosaic trisomy 18 case with long term survive
PP73. Pehlivan D., Ozturk S., Cefle K., Duman N., Palanduz S. - Istanbul, Turkey
Stickler syndrome: First case from Türkiye
PP74. Severin E., Albu C., Albu D.F. - Bucharest, Romania
Hyperdontia: isolated or associated with genetic syndromes
PP75. Vazharova R., Dimova I., Zaharieva B., Tincheva R., Hristov G., Toncheva D. - Sofia, Bulgaria
Detection of microdeletions in patients affected with congenital heart abnormalities
PP76. Zisovska E., Lazovska B. – Skopje, Republic of Macedonia
Down Syndrome - The Incidence and Risks
PP77. Zisovska E., Lazovska B – Skopje, Republic of Macedonia
Dysmorphia -The main suspicion for chromosomal abnormality
PP78. Sukarova Angelovska E., Ilieva G, Sredovska A, Kocova M – Skopje R. Macedonia
The importance of fluorescent in situ hubridization (FISH) in detecting microdeletion syndromes
PP79. Tasic V. – Skopje, R. Macedonia
Report from Macedonia on new entity-Dent 2 disease
PP80. Tasic V., Jancevska A., Sofijanova A., Trajkovski Z., Misevska L., Ristoska Bojkovska N., Gucev Z. – Skopje, R. Macedonia
– Skopje, R. Macedonia
Renal status in children with VACTERL association
PP81. Zeynel S., Gucev Z., Laban Guceva N., Jancevska A., Korneti P., Ristoska Bojkovska N., Tasic V. – Skopje, R. Macedonia
Renal dysplasia in Bardet-Biedl syndrome
PP82. Cefle A., Cefle K., Pehlivan D. - Istanbul, Turkey
Two siblings with multiple exostoses
- MOLECULAR BASIS OF MONOGENIC AND COMPLEX DISEASES
PP83. Bordea C., Gaina G., Mihalcea A., Costache M., Ionica E. - Bucharest, Romania
Molecular biology analyses on muscular dystrophies
PP84. Todorova A., Bogdanova N., Kremensky I., Horst J., Dworniczak B. - Sofia, Bulgaria
MLPA analysis for deletions/duplications detection in Bulgarian DMD/BMD patients
PP85. Lalic T., Vossen R.H.A.M., Coffa J., Schouten J.P., Guc-Scekic M., Radivojevic D., Djurisic M., Breuning M.H., White S.J., den Dunnen J.T. - Belgrade, Serbia
Deletions and duplications in the dystrophin gene: retrospective MLPA analyses show complex rearrangements and previously undetected deletions
PP86. Georgieva B., Todorova A. , Todorov T. , Tournev I. , Kremensky I. , Mitev V. - Sofia, Bulgaria
Limb-Girdle Muscular Dystrophy Type 2A (LGMD2A, Calpainopathy) In Bulgaria
PP87. Latypova E., Krupina N., Magzhanov R., Khusnutdinova E., Khidiyatova I.- Ufa, Russia
Duplication frequency analysis of PMP22 gene in hereditary motor and sensory neuropathy patients from Bashkortostan
PP88. Todorov Tihomir, Todorova A., Halliger-Keller B., Kress W., Tournev I., Dabauvalle M-C., Kremensky I., Mueller C.R. - Sofia, Bulgaria
Spectrum of mutations in the LMNA gene, causing muscular dystrophy with conduction system disease (EDMD-AD or LGMD1B
PP89. Apostol P., Cimponeriu D., Butoianu N., Stavarachi M., Toma M., Magureanu S., Gavrila L. - Bucharest, Romania
The molecular analysis of mutations in SMN, NAIP and TGFB genes in Romanian SMA patients
PP90. Ebru E., Berilgen S., Demir D., Elyas H., Mungen B. - Elazig, Turkey
The association between uncoupling protein 2 (UPC2) gene exon 8 deletion
PP91. Islamgulov D., , Karunas A., Khusnutdinova E. - Ufa, Russia
Analysis of premutations in the FMR1 gene in Parkinson's disease
PP92. Yordanova I., Mehrbian S., Genova J., Raycheva M., Kremensky I., Traykov L., Jordanova A. - Sofia, Bulgaria
Apolipoprotein E and Alzheimer disease in Bulgarian patients
PP93. Yilmaz E.D., Kurt E., Oktar S., Tekedereli I., Gumus G., Bilgic V., Gazi Alatas N.A., Yuce H.- Elazig, Turkey
No association between catalase gene polymorphism, −262C→T, and bipolar mood disorder
PP94. Faskhutdinova G., Juriev E., Gaysina D., Zainullina A., Khusnutdinova E. - Ufa, Russia
The serotonin transporter gene: analysis of haplotypes in substance abuse
PP95. Noskova T., Gaysina D., Zainullina A., Khusnutdinova E. - Ufa, Russia
Haplotype analysis of the serotonin transporter gene with major depressive disorder in Bashkortostan
PP96. Gaysina D., Zainullina A., Khusnutdinova E. - Ufa, Russia
Association study of X chromosome located genes of serotonergic system with suicidal behavior
PP97. Bilge E., Kucukali I.C., Ozkok E., Aydin M., Tekin D., Ozbek Z., Kara I. - Istanbul, Turkey
Role of matrix metalloproteinase-3 in bipolar affective disorder
PP98. Tekedereli I., Ilhan A., Yuce H., Isik B., Alacam H., Elyas H., Akyol O. - Elazig, Turkey
Mitochondrial targeting sequence polymorphism of manganese superoxide dismutase (SOD2) in patients with migraine
PP99. Todorov Theodor, Savov A., Mihaylova V., Krustev Z., Jelev H., Tournev I., Penkov V., Konstantinova D., Tankova Lj., Tzolova N. Kremensky - Sofia, Bulgaria
Novel ethnic specific mutations in Bulgarian patients with Wilson disease
PP100. Kara M., Tekedereli I., Kara B., Atmaca M., Elyas H. - Elazig, Turkey
Relationship between body dysmorphic disorder and genetic polymorphism of catalase: a preliminary study
PP101. Gorovenko N.G., Rossokha Z.I., Podolskaya S.V. - Shupyk, Ukraine
Genetic polymorphism of glutathione-S-transferase T1 and M1 in the newborns with infant respiratory distress syndrome (IRDS) in Ukrainian population
PP102. Izmaylova A., Karunas A., Khuzina A., Zagidullin S., Khusnutdinova E. - Ufa, Russia
The analysis of cytokine genes polymorphism in asthma patients and healthy donors from Volga-Ural region of Russia
PP103. Radivojevic D., Djurisic M., Lalic T., Guc-Scekic M., Minic P., Sovtic A., Tzetis M., Kanavakis E. - Belgrade, Serbia
Identification of complex alleles in two cystic fibrosis patients from Serbia and Montenegro
PP104. Popovic-Kuzmanovic D., Novakovic I., Mikovic D., Maksimovic N., Stojanovic Lj., Mirkovic D., Lukovic Lj, Aksentijevic I., Krajinovic M.- Belgrade, Serbia
Possible familial antiphospholipid syndrome - case study
PP105. Stankovic M., Rakicevic Lj., Mitic-Milikic M., Nagorni-Obradovic Lj., Petrovic-Stanojevic N., Andjelic M., Dopudja-Pantic V., Surlan M., Vujicic I., Ponomarov D., Radojkovic D. - Belgrade, Serbia
Matrix metalloproteinase polymorphisms in patients with COPD
PP106. Timasheva Y.R., Nasibullin T.R., Zakirova A.N., Mustafina O.E. - Ufa, Russia
Association of cytokine genes polymorphisms with essential hypertension in Tatars from Russia
PP107. Tazetdinov A., Dzhemileva L., Ponidelko S., Khusnutdinova E. - Ufa, Russia
Molecular analysis of MTRNR1 and MTTS1 genes in patients with suddenly deafness from Russia
PP108. Sharipova E., Aznabaeva L., Arefyeva N., Zainullina A., Khusnutdinova E.- Ufa, Russia
Polymorphisms of the interleukin-1 receptor antagonist gene and the interleukin-1β gene in patients with chronic rhinosinusitis from Bashkortostan
PP109. Khuzina A., Karunas A., Biktasheva A., Yuldasheva A., Etkina E., Khusnutdinova E. - Ufa, Russia
Association analysis of the interferon-gamma gene polymorphism with allergic rhinitis in Volga-Ural region of Russia
PP110. Stoyanova V., Ghenev E., Zhelev N. - Plovdiv, Bugaria
Investigation on the expression of protein p53 in the development of left ventricular hypertrophy in rats
PP111. Danilova V.V., Tuktarova I.A., Asilguzhina A.Kh., Mustafina O.E. - Ufa, Russia
Polymorphism of candidates cardiovascular diseases genes in Tatars with age gradation
PP112. Tulyakova G., Nasibullin T., Zakirova A., Khusnutdinova E., Mustafina O., Salmanov A. - Ufa, Russia
Gene polymorphisms in the Interleykin-1 locus and the risk of myocardial infarction
PP113. Balhiyarova Z., Morugova T., Avzaletdinova D., Mustafina O. - Ufa, Russia
The IL6 -572G/C and IL12B -1159C/A polymorphisms and type 1 diabetes mellitus in Tatars of Bashkortostan
PP114. Cimponeriu D., Ungureanu F.D., Moldovan C., Apostol P., Serafinceanu C., Craciun A.M., Radu I., Stavarachi M., Mihai T., Usurelu D., Dan L. , Cherry L., Dumitrescu L., L Gavrila L., Cheta D. - Bucharest, Romania
The MTHFR C677T polymorphism increases the risk for ESRD in Romanian diabetic and nondiabetic patients
PP115. Maksimovic N., Jovicic S., Mirkovic D., Novakovic I., Simic-Ogrizovic S. - Belgrade, Serbia
MTHFR gene polymorphisms in renal transplanted patients
PP116. Nestorovic A., Djordjevic V., Ljujic M., Ristanovic M., Tulic C., Radunovic N., Vasiljevic M., Nikolic A. - Belgrade, Serbia
MTHFR C677T mutation and male infertility in Serbia
PP117. Zainullin I., Kulavsky V., Zainullina A., Khusnutdinova E. - Ufa, Russia
Analysis of MTHFR, ENOS and TPA genes polymorphisms in women with preeclampsia from Russia
PP118. Savov A., Koleva R., Dimitrova V., Nikolova D., Chernev T., Kremensky I. - Sofia, Bulgaria
The impact of inherited thrombophilia on the development of some pregnancy complications
PP119. Laudy Cherry, Letitia Dan, Rodica Talmaci, Daniel Coriu, Cimponeriu Danut, Pompilia Apostol, Dana Usurelu, Lucian Gavrila - Bucharest, Romania
A rare worldwide mutation was added to the mutational spectrum of β globin gene in the Romanian population
PP120. Stanojevic E., Glamocanin S., Plaseska-Karanfilska D. Efremov G.D. - Skopje
R. Macedonia
Compound heterozygosity for hemoglobin Knossos and IVS-I-6 mutation in a
Macedonian boy
PP121. Pavlovic S., Petrucev B., Tosic N., Stojiljkovic M., Karan-Djurasevic T., Kostic T.- Belgrade, Serbia
Haplotype diversity of beta-globin genes in Serbia
PP122. Kochetova O.V. - Ufa, Russia
The CYP1A2 and NQO1 genotypes are possible factors causing chemical induced abnormal liver function
PP123. Anastasovska V., Koceva S., Kocova M. - Skopje R. Macedonia
Detection of CYP21 mutations in congenital adrenal hyperplasia
PP124. Plaseska-Karanfilska D., Novevski P., Kuzevska K., Basevska N., Kocova M., Efremov G.D. – Skopje, R. Macedonia
A new familial mutation in the SRY gene (Arg133Gly)
PP125. Popovska-Jankovic K., Tasic V., Bogdanovic R., Miljkovic P., Baskin E., Efremov G.D., Plaseska-Karanfilska D. – Skopje, R. Macedonia
Five novel mutations in cystinuria genes SLC3A1 and SLC7A9
PP126. Uzumcu A., Uyguner O., Ulubil-Emiroglu M., Hafiz G., Baserer N., Eris H., Basaran S., Wollnik B. - Istanbul, Turkey
Compound heterozygosity for novel and known mutations in SLC26A4 cause large vestibular aqueduct
PP127. Yuce H., Hepsen F., Tekedereli I., Keskin U.C., Elyas H., Akyol O. - Elazig, Turkey
Lack of association between pseudoexfoliation syndrome and manganese superoxide dismutase polymorphism
PP128. Etem E., Kökcam I., Oguz S., Elyas H., Etem A. - Elazıg, Turkey
The investigation of TLR2 gene polymophism in acne patients
PP129. Peova S., Stavric K., Kareva L., Mironska K. - Skopje, R. Macedonia
Hyper-IgD syndrome
PP130. Peova S., Mironska K., Kareva L., Stavric K. - Skopje, R. Macedonia
Mutation analysis of the BTK gene in patients with X-linked gammaglobulinemia in Macedonia
PP131. Gucev Z., Le Bouc Y., Godeau F., Jovanov G., Jancevska A. - Skopje, R. Macedonia
Insulin-like growth factor binding protein-3, It's proteolytic fragments and their significance
- GENOMICS & PROTEOMICS, HIGH THROUGHOUT TECHNOLOGY
PP132. Kastrin A, Peterlin B. – Ljubljana, Slovenia
Mining gene expression data from multiple microarray studies using gene ontology annotation: application to neurodegenerative disorders
PP133. Djurovic J., Petrovic I., Seovic M., Stevanovic M. - Belgrade, Serbia
Mapping of the positive control elements within human SOX14 promoter
PP134. Kovacevic-Grujicic N., Mojsin M., Stevanović M. - Belgrade, Serbia
The zinc finger transcription factor ZBP-89 is a repressor of the human SOX3 gene
PP135. Savic T., Nikčević G., Stevanović M. - Belgrade, Serbia
Delineation of the novel response region that mediates a stimulatory effect of retinoic acid on SOX3 gene expression
PP136. Krstic A., Stevanovic M. - Belgrade, Serbia
Involvement of NF-Y in transcriptional regulation of the human SOX3 gene
PP137. Nikčević G., Mojsin M., Kovačević Grujičić N., Krstić A., Savić T., Stevanović M. - Belgrade, Serbia
Human SOX3 gene: mapping of the elements involved in retinoic acid induced transcriptional activation
- GENETIC EPIDEMIOLOGY AND POPULATION GENETIC & DIVERSITY
PP138. Nossikoff A., Vikentieva E., Savov A., Dimitrov S., Kremensky I., Baleva M., Denchev S.- Sofia, Bulgaria
Lack of associaciation between factor V Leiden mutation and 20210 G/A mutation of the prothrombin gene and myocardial infarction in Bulgarian population
PP139. Menevse S.E., Alp E., Tulmac M., Kan D., Cengel A., Yalcın R. - Ankara, Turkey
eNOS and MMP-9 gene polymorphisms association with coronary artery disease in Turkish population
PP140. Nossikoff A., Vikentieva E., Savov A., Dimitrov S., Bjanov K., Kremensky I., Baleva M., Denchev S. - Sofia, Bulgaria
4G/5G polymorphism in the promoter region of the PAI-1 gene in patients with myocardial infarction in Bulgaria - A pilot case-control study
PP141. Gunay M., Ulkuer M.K., Ulkuer U., Gokdemir K., Karaoguz M.Y., Çetin E., Alp E., Kesici T. - Ankara, Turkey
The angiotensin converting enzyme I/D gene polymorphism in elite Turkish athletes
PP142. Orhan N., Kucukali C.I., Zengin A., Aydin M., Ozkok E., Kara I. - Istanbul, Turkey
Are angiotensin-converting enzyme gene variations risk factor for development of schizophrenia?
PP143. Ozbey U., Etem E., Yuce H. - Elazig, Turkey
Insertion/deletion polymorphism of the angiotensin converting enzyme gene in patients of migraine with aura and migraine without aura
PP144. Baltova S., Popova I. - Plovdiv, Bulgaria
Polymorphism of erythrocyte glyoxalase (GLO-I E.C.4.4.1.5) in the Bulgarian population from south-central and south-eastern region in Bulgaria
PP145. Sokolova M.V., Rebrikov D.V., Borodina T.A., Kozlov A.I., Borinskaya S.A., Yankovsky N.K - Moscow, Russia
Hypolactasia-associated polymorphism in lactase gene LCT C/T-13910 in populations of Russia and neighboring countries
PP146. Djordjevic V., Rakicevic Lj., Tomic B., Miljic P., Mikovic D., Kovac M., Antonijevic N., Radojkovic D. - Belgrade, Serbia
Recurrent miscarriages and maternal thrombophilia in Serbian population
PP147. Ristanovic M., Nikolic A., Radojkovic D.- Belgrade, Serbia
Genetic testing in infertile men in Serbia
PP148. Novevski P., Plaseski T., Kocevska B., Dimitrovski C., Efremov G.D. Plaseska-Karanfilska D. – Skopje, R. Macedonia
Associatiation between polymorphism of the mitochondrial DNA polymerase gamma gene (POLG) and male infertility among Macedonian population
PP149. Menevse A., Baysal E., Yilmaz A., Bayazit Y.A., Altinyay S., Gunduz B., Goksu N., Menevse S. - Ankara, Turkey
Frequency of the 35delG and del120E mutations in the GJB2 gene in Turkish families with non-syndromic hearing loss
PP150. Momirovska A., Sukarova Stefanovska E., Efremov G. - Skopje, Macedonia
Connexin 26 mutations in nonsyndromic deafness in Republic of Macedonia
PP151. Ivanova M., Chorbov V., Kostov C., Milanova V., Kremensky I., Kaneva R. - Sofia, Bulgaria
Polymorphisms in serotonine and dopamine related genes and their relationship to personality traits in Bulgarian subjects
PP152. Voinova-Ulas V.Y., Iourov I.Y., Novikov P.V., Vorsanova S.G. - Moscow, Russia
Population-based estimation of X-linked mental retardation frequency in Russia
PP153. Trajkov D., Strezova A, Petlichkovski A, Arsov T, Efinska-Mladenovska O, Trajchevska M, Spiroski M - Skopje, R. Macedonia
Cytokine gene polymorphism in Macedonian patients with tuberculosis
PP154. Atanasovska-Stojanovska A., Popovska M., Angelovska L., Trajkov D., Arsov T., Petlichkovski A., Strezova A., Efinska-Mladenovska O., Spiroski M. – Skopje, R. Macedonia
Association of Cytokine Gene Polymorphism with Periodontitis in the Macedonian Population
PP155. Spiroska E., Hristomanova S., Trajkov D., Arsov T., Petlichkovski A., Strezova A., Efinska-Mladenovska O., Spiroski M. - Skopje, R. Macedonia
Killer IG-like receptor (KIR) gene polymorphism in the Macedonian population
PP156. Zaharova B., Kremensky I.- Sofia, Bulgaria
Heterogeneous structure of Bulgarian population revealed by DNA analysis of 17 highly polymorphic loci
PP157. Talaganova S., Trivodalieva S., Arsovska S., Kaeva M., Efremov G.D., Plaseska-Karanfilska D. – Skopje, R. Macedonia
The parental and meiotic origin of extra chromosome 21 in Down syndrome patients
PP158. Tosheska-Trajkovska K, Labudovic D, Alabakovska S, Todorova B, Skopje, R. Macedonia
Phenotypic expression of Apo(a) in Macedonian children
PP159. Davalieva K., Efremov G. D., Plaseska-Karanfilska D.- Skopje, Macedonia
Determination of fetal sex by real-time PCR analysis of SRY gene in maternal blood
PP160. Bocic M., Drakulić D., Seović M., Sretenović Z., Stevanović M. - Belgrade, Serbia
Rapid prenatal diagnosis of most common numeric chromosomal abnormalities on uncultured amniotic fluid using fluorescent in situ hybridization (FISH)
PP161. Stefanovska A-M., Anevska A., Popovic M., Ivanovski M., Adamoska-Klisaroska S., Vasilevska M., Lazarevski S. - Skopje, R. Macedonia
Prenatal karyotypes of fetuses conceived by assisted reproductive treatment
PP162. Raynova R., Kremensky I., Andonova S.- Sofia, Bulgaria
QF-PCR analysis and indications for invasive prenatal procedures
PP163. Kocheva S.A., Plaseska-Karanfilska D. , Vlaski-Jekic S., Kuturec M. and Efremov G.D. - Skopje R. Macedonia
Genetic counseling and prenatal diagnosis in Macedonian DMD/BMD families
PP164. Deveci D., Yuce H. - Elazig, Turkey
Complete trisomy 15 in fetal tissue
PP165. Deveci D., Yuce H., Etem E.- Elazig, Turkey
Prenatal diagnosis of homozygosity for pericentric inversions of chromosome 9 with one case
PP166. Miskovic M., Cirkovic S., Krstic A., Guc-Scekic M.- Belgrade, Serbia
Case report: enlarged acrocentric p-arm of chromosome 22: cryptic translocation or normal polymorphism in fetal karyotype?
PP167. Alby C., Albu D.F., Severin E. - Bucharest, Romania
Prenatal diagnosis of a fetus with Lip-Jaw-palatal cleft
PP168. Dimcev P., Petanovski Z., Stojkovski J., Efremovski J. - Skopje, Macedonia
Screening for chromosomal defects with ultrasound markers
PP169. Albu D.F., Severin E., Albu C., Toma A.- Bucharest, Romania
Fetal thanatophoric dysplasia - second trimester ultrasound examination
PP170. Sinigerska I., Hassanova I., Vladimirova K., Kremensky I. - Sofia, Bulgaria
Enzymatic diagnosis of lysosmal storage diseases in Bulgaria
- GENETIC SERVICES IN BALKAN COUNTRIES
PP171. Ivanova M., Sinigerska I., Kremensky I. - Sofia, Bulgaria
Diagnosis of inherited metabolic diseases in Bulgaria
PP172. Kocova M., Anastasovska V., Sukarova-Angelovska E., Gjurkova B. - Skopje, R. Macedonia
Neonatal thyroid screening in The Republic of Macedonia
- GENETIC COUNSELING, GENETIC EDUCATION AND BIOETHICS
PP173. Kovacevic L. Bakal N., Marjanovic D. - Sarajevo, Bosnia and Herzegovina
Ethical issuess of interpretation a final report in DNA identification - case study
- THERAPY FOR GENETIC DISORDERS
PP174. Malinkova R.M. - Samarkand, Uzbekistan
The efficiency of substitutive hormonal therapy of Femoston by dysgenesis of Gonads
PP175. Özkaynakçı A.E., D. Sevinç D., Özkara Ç, Uzan M., Koçer A., Aker R., Ulucan K., Gören M.Z., Küçükibrahimoğlu E., Bircan R., Özyurt H.B., Güney A.İ., Onat F.
CYP2C9 and CYP2C19 Polymorphisms In Patients Under Phenytoin Therapy
PP176. Saraeva R., Paskaleva I., Eap C., Ganev V. - Sofia, Bulgaria
Pharmacogenetics of acenocoumarol - CYP2C9, CYP2C19, CYP1A2, CYP3A4/5 and MDR1 gene polymorphisms and dose requirements
PP177. Baran Y., Gündüz U., Ural A.U., Öğretmen B. - Ankara, Turkey
Apoptotic pathways induced by imatinib in sensitive and imatinib-resistant k562 cells
PP178. Baran Y., Gündüz U., Bielawski J., Öğretmen B. - Ankara, Turkey
Circumventing multi-drug resistance by a combination therapy of imatinib and gcs inhibitor in imatinib-resistant human chronic myeloid leukemia cells
PP179. Baran Y., Gündüz U., Öğretmen B. - Ankara, Turkey
The sequence analyses of Imatinib Mesylate binding site of ABL kinase domain in sensitive and Imatinib-resistant human CML cells
PP180. Renata Jankova-Ajanovska, Zlatko Jakovski Biljana Janeska, Aleksej Duma – Skopje, Republic of Macedonia
A microvariant allele FGA*22.2 in one case in Republic of Macedonia
PP181. Grigor Zoraqi, Ela Hysa, Daniele Podini – Tirana, Albania
Allele frequencies for the AmpFlSTR Identifiler in an Albanian population sample
PP182. Grigor Zoraqi, Lila Shundi, Eleni Anastasi, Etleva Refatllari, Halim Kosova – Tirana, Albania
Determination of beta-globin alleles in Albanian thalassemic patients of the Pediatric Hospital of Tirana
PP183. Grigor Zoraqi, Lila Shundi, Evda Vevecka, Halim Kosova – Tirana, Albania
Cistic Fibrosis mutation testing in Albania |
