Showing results (11-20 of 56) with videos related to
Sort By:
Pageof 6
Genetic Testing and Molecular Biomarkers|October 8, 2011
The rate of sex chromosome aneuploidies in prenatal diagnosis and subsequent decisions in Western TurkeyEsra Ataman, Ozgur Cogulu, Asude Durmaz, et al.Hematology (Amsterdam, Netherlands)|October 15, 2014
Molecular analysis of abnormal hemoglobins in beta chain in Aegean region of Turkey and first reports of hemoglobin Andrew-Minneapolis and Hb Hinsdale from TurkeyAyça Aykut, Hüseyin Onay, Asude Durmaz, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2022
Association between clinical variations and copy number variations in cases with Turner syndromeEzgi Aksoy, Ozgur Cogulu, Erhan Pariltay, et al.Cancer Genetics|July 17, 2022
Complex karyotype with double Philadelphia chromosome and T315I mutation results in blastic phase and extensive extramedullary infiltration in a chronic myeloid leukemia patientEren Arslan Davulcu, Mert Pekerbas, Emin Karaca, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|July 16, 2014
Two novel mutations in acid α-glucosidase gene in two patients with Pompe diseaseAyca Aykut, Huseyin Onay, Melis Kose, et al.Cancer Genetics|August 7, 2024
A complex t(15;22;17)(q22;q11.2;q21) variant of APLBilgesu Ak, Özge Güngör, Emin Karaca, et al.Hemoglobin|August 22, 2023
Successful Treatment of a Child with Hemoglobin Hammersmith with Hematopoietic Stem Cell TransplantationAyşen Türedi Yıldırım, Hüseyin Gülen, Hülya Türkmen, et al.Journal of Assisted Reproduction and Genetics|October 17, 2025
Identifying a rare mechanism: double parallel trisomy rescue leading to combined segmental and whole-chromosome mosaicism in an IVF-derived embryoElif Kubar, Alp Peker, İrem Oflaz, et al.Asian Pacific Journal of Allergy and Immunology|February 27, 2021
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literatureElif Azarsiz, Neslihan Karaca, Emin Karaca, et al.Clinical Dysmorphology|June 3, 2005
Trigonocephaly and Wilson's disease in two siblingsOzgur Cogulu, Huseyin Onay, Funda Ozgenc, et al.Pageof 6