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Evidence that the wider social environment moderates the association between familial liability and psychosis spectrum outcome
Author / Creator:Binbay, T. ; Drukker, M. ; Alptekin, K. ; Elbi, H. ; Tanık, F. Aksu ; Özkınay, F. ; Onay, H. ; Zağlı, N. ; van Os, J.
Publisher:Cambridge, UK: Cambridge University Press
Journal title:Psychological medicine, 2012-12, Vol.42 (12), p.2499-2510
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Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss
Author / Creator:Bademci, G. ; Cengiz, F. B. ; Foster II, J. ; Duman, D. ; Sennaroglu, L. ; Diaz-Horta, O. ; Atik, T. ; Kirazli, T. ; Olgun, L. ; Alper, H. ; Menendez, I. ; Loclar, I. ; Sennaroglu, G. ; Tokgoz-Yilmaz, S. ; Guo, S. ; Olgun, Y. ; Mahdieh, N. ; Bonyadi, M. ; Bozan, N. ; Ayral, A. ; Ozkinay, F. ; Yildirim-Baylan, M. ; Blanton, S. H. ; Tekin, M.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2016-08, Vol.6 (1), p.31622-31622, Article 31622
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In vitro gene manipulation of spinal muscular atrophy fibroblast cell line using gene-targeting fragment for restoration of SMN protein expression
Author / Creator:Rashnonejad, A ; Gündüz, C ; Süslüer, S Y ; Onay, H ; Durmaz, B ; Bandehpour, M ; Özkınay, F
Publisher:London: Nature Publishing Group UK
Journal title:Gene therapy, 2016-01, Vol.23 (1), p.10-17
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558 Prader-Willi Syndrome Due to Maternal Uniparental Disomy following Assisted Reproductive Technology
Author / Creator:Cogulu, O ; Atik, T ; Karaca, E ; Onay, H ; Ozkinay, F
Publisher:London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health
Journal title:Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A162-A162
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Low levels of mannose-binding lectin confers protection against tuberculosis in Turkish children
Author / Creator:Cosar, H ; Ozkinay, F ; Onay, H ; Bayram, N ; Bakiler, A. R ; Anıl, M ; Can, D ; Özkınay, C
Publisher:Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag
Journal title:European journal of clinical microbiology & infectious diseases, 2008-12, Vol.27 (12), p.1165-1169
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GENETIC COUNSELLING IN FEINGOLD SYNDROME AND A NOVEL MUTATION
Author / Creator:Atik, T ; Güvenç, M S ; Onay, H ; Özkinay, F ; Çoğulu, Ö
Publisher:Switzerland: Éditions Médecine et Hygiène
Journal title:Genetic counseling, 2016-01, Vol.27 (3), p.381-384
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A FURTHER PATIENT OF PURE 15q DELETION: CLINICAL AND MOLECULAR CYTOGENETIC FINDINGS
Author / Creator:Solmaz, A Ece ; Durmaz, B ; Braekeleer, M D ; Cogulu, O ; Ozkinay, F
Publisher:Switzerland: Éditions Médecine et Hygiène
Journal title:Genetic counseling, 2016, Vol.27 (1), p.1-8
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TWINS WITH KLEEFSTRA SYNDROME DUE TO CHROMOSOME 9q34.3 MICRODELETION
Author / Creator:Atik, T ; Karaca, E ; Ozkinay, E ; Cogulu, O
Publisher:Switzerland: Éditions Médecine et Hygiène
Journal title:Genetic counseling, 2015-01, Vol.26 (4), p.431-435
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RESULTS OF FIFTEEN-YEAR FOLLOW-UP FROM A SINGLE CENTER: FINDINGS AND RISKS FOR TUMOR DEVELOPMENT IN ISOLATED HEMIHYPERPLASIA CASES
Author / Creator:ATIK, T ; COGULU, O ; OZKINAY, F
Publisher:Genève: Médecine & hygiène
Journal title:Genetic counseling, 2014-01, Vol.25 (4), p.417-421
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Transmembrane Activator and Caml Interactor (Taci) Haploinsufficiency in B-Cell Dysfunction in a Patient with Smith-Magenis Syndrome
Author / Creator:Karaca, E ; Atik, T ; Alpman Durmaz, A ; Ozkinay, F ; Cogulu, O
Publisher:Switzerland: Éditions Médecine et Hygiène
Journal title:Genetic counseling, 2016-01, Vol.27 (2), p.251
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CONGENITAL ABSENCE OF THE PORTAL VEIN IN A CHILD WITH TURNER SYNDROME
Author / Creator:Sahin, Ö N Atan ; Atik, T ; Özkinay, F
Publisher:Switzerland: Éditions Médecine et Hygiène
Journal title:Genetic counseling, 2015-01, Vol.26 (3), p.353
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61 Association of Vitamin D Receptor Gene Polymorphisms and Bronchopulmonary Dysplasia
Author / Creator:Koroglu, O Altun ; Onay, H ; Cakmak, B ; Bilgin, B ; Yalaz, M ; Tunc, S ; Ozkinay, F ; Kultursay, N
Publisher:London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health
Journal title:Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A17-A18
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DETERMINATION OF FETAL RHESUS D STATUS BY MATERNAL PLASMA DNA ANALYSIS
Author / Creator:Aykut, A. ; Onay, H. ; Gunduz, C. ; Ozkinay, F. ; Cogulu, O. ; Sagol, S.
Publisher:Macedonia: De Gruyter Open
Journal title:Balkan journal of medical genetics, 2013-12, Vol.16 (2), p.33-38
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Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: Report and review
Author / Creator:Akgul, M. ; Ozkinay, F. ; Ercal, D. ; Cogulu, O. ; Dogan, O. ; Altay, B. ; Tavmergen, E. ; Gunduz, C. ; Ozkinay, C.
Publisher:Boston: Springer US
Journal title:Journal of assisted reproduction and genetics, 2009-03, Vol.26 (2-3), p.119-122
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Pontocerebellar hypoplasia type III (CLAM): Extended phenotype and novel molecular findings
Author / Creator:Durmaz, B. ; Wollnik, B. ; Cogulu, O. ; Li, Y. ; Tekgul, H. ; Hazan, F. ; Ozkinay, F.
Publisher:Darmstadt: Steinkopff-Verlag
Journal title:Journal of neurology, 2009-03, Vol.256 (3), p.416-419
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252 Whole Genome Microrna Expression Profiling in Childhood Acute Lymphoblastic Leukemia: A Prospective Evaluation
Author / Creator:Duyu, M ; Cogulu, O ; Durmaz, B ; Gunduz, C ; Vergin, C ; Karapinar, D Yilmaz ; Aksoylar, S ; Kavakli, K ; Cetingul, N ; Irken, G ; Yaman, Y ; Ozkinay, F
Publisher:London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health
Journal title:Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A73-A73
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THE SPECTRUM OF CLINICAL FEATURES ASSOCIATED WITH KLIPPEL-TRENAUNAY-WEBER SYNDROME
Author / Creator:Sahin, O N Atan ; Atik, T ; Coğulu, O ; Ozkinay, F
Publisher:Switzerland: Éditions Médecine et Hygiène
Journal title:Genetic counseling, 2015-01, Vol.26 (2), p.249-251
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Mosaic trisomy 8 syndrome with a novel finding of ectopic kidney
Author / Creator:Aykut, A ; Cogulu, O ; Ozkinay, F
Publisher:Switzerland: Éditions Médecine et Hygiène
Journal title:Genetic counseling, 2012, Vol.23 (1), p.77
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A TWIN SIBLING WITH PRADER-WILLI SYNDROME CAUSED BY UNIPARENTAL DISOMY CONCEIVED AFTER IN VITRO FERTILIZATION
Author / Creator:ATIK, T ; AYKUT, A ; KARACA, E ; ONAY, H ; OZKINAY, F ; COGULU, O
Publisher:Genève: Médecine & hygiène
Journal title:Genetic counseling, 2014-01, Vol.25 (4), p.433-437
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EVALUATION OF PREIMPLANTATION GENETIC ANEUPLOIDY SCREENING CASES AT A REFERENCE GENETICS CENTER: 10 YEARS' EXPERIENCE
Author / Creator:Durmaz, B ; Karaca, E ; Tavmergen Goker, E N ; Tavmergen, E ; Sahin, G ; Akdogan, A ; Yasar, B P ; Gunduz, C ; Ozkinay, R
Publisher:Switzerland: Éditions Médecine et Hygiène
Journal title:Genetic counseling, 2016-01, Vol.27 (4), p.461-470
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Showing 1 to 20 of 54 results

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Evidence that the wider social environment moderates the association between familial liability and psychosis spectrum outcome

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Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss

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In vitro gene manipulation of spinal muscular atrophy fibroblast cell line using gene-targeting fragment for restoration of SMN protein expression

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558 Prader-Willi Syndrome Due to Maternal Uniparental Disomy following Assisted Reproductive Technology

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Low levels of mannose-binding lectin confers protection against tuberculosis in Turkish children

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GENETIC COUNSELLING IN FEINGOLD SYNDROME AND A NOVEL MUTATION

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A FURTHER PATIENT OF PURE 15q DELETION: CLINICAL AND MOLECULAR CYTOGENETIC FINDINGS

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TWINS WITH KLEEFSTRA SYNDROME DUE TO CHROMOSOME 9q34.3 MICRODELETION

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RESULTS OF FIFTEEN-YEAR FOLLOW-UP FROM A SINGLE CENTER: FINDINGS AND RISKS FOR TUMOR DEVELOPMENT IN ISOLATED HEMIHYPERPLASIA CASES

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Transmembrane Activator and Caml Interactor (Taci) Haploinsufficiency in B-Cell Dysfunction in a Patient with Smith-Magenis Syndrome

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CONGENITAL ABSENCE OF THE PORTAL VEIN IN A CHILD WITH TURNER SYNDROME

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61 Association of Vitamin D Receptor Gene Polymorphisms and Bronchopulmonary Dysplasia

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DETERMINATION OF FETAL RHESUS D STATUS BY MATERNAL PLASMA DNA ANALYSIS

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Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: Report and review

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Pontocerebellar hypoplasia type III (CLAM): Extended phenotype and novel molecular findings

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252 Whole Genome Microrna Expression Profiling in Childhood Acute Lymphoblastic Leukemia: A Prospective Evaluation

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THE SPECTRUM OF CLINICAL FEATURES ASSOCIATED WITH KLIPPEL-TRENAUNAY-WEBER SYNDROME

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Mosaic trisomy 8 syndrome with a novel finding of ectopic kidney

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A TWIN SIBLING WITH PRADER-WILLI SYNDROME CAUSED BY UNIPARENTAL DISOMY CONCEIVED AFTER IN VITRO FERTILIZATION

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EVALUATION OF PREIMPLANTATION GENETIC ANEUPLOIDY SCREENING CASES AT A REFERENCE GENETICS CENTER: 10 YEARS' EXPERIENCE

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