Showing results (11-20 of 35) with videos related to
Sort By:
Pageof 4
Reproductive Biomedicine Online|March 15, 2008
CYP1A1 gene polymorphism and polycystic ovary syndromeIbrahim Esinler, Dilek Aktas, Umit Otegen, et al.Nephrology (Carlton, Vic.)|May 4, 2006
Rare case of Alstrom syndrome without obesity and with short stature, diagnosed in adulthoodEyup Koç, Gulden Bayrak, Murat Suher, et al.Molecular Diagnosis & Therapy|August 16, 2017
Prospective Turkish Cohort Study to Investigate the Frequency of Niemann-Pick Disease Type C Mutations in Consanguineous Families with at Least One Homozygous Family MemberMeral Topçu, Dilek Aktas, Merih Öztoprak, et al.Gynecologic Oncology|January 13, 2006
CYP1A1 gene polymorphism as a risk factor for cervical intraepithelial neoplasia and invasive cervical cancerCagatay Taskiran, Dilek Aktas, Nilufer Yigit-Celik, et al.Developmental Medicine and Child Neurology|March 16, 2007
Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3)Sevim Balci, Aysun Unal, Ozlem Engiz, et al.Pediatric Blood & Cancer|April 18, 2009
Wilms tumor, AML and medulloblastoma in a child with cancer prone syndrome of total premature chromatid separation and Fanconi anemiaNeriman Sari, Canan Akyuz, Dilek Aktas, et al.European Journal of Medical Genetics|April 29, 2008
Cryptic trisomy 5q35.2qter and deletion 1p36.3 characterised using FISH and array-based CGHEda G Utine, Yasemin Alanay, Dilek Aktas, et al.Molecular Cytogenetics|July 2, 2009
Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case reportDilek Aktas, Anja Weise, Eda Utine, et al.Journal of Child Neurology|April 25, 2013
A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophyG Eda Utine, Göknur Haliloğlu, Bilge Salanci, et al.European Journal of Human Genetics : EJHG|March 9, 2017
European registration process for Clinical Laboratory Geneticists in genetic healthcareThomas Liehr, Isabel M Carreira, Dilek Aktas, et al.Pageof 4