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Fetal and Pediatric Pathology|April 4, 2012
A novel aspartoacylase (ASPA) gene mutation in Canavan diseaseAsude Alpman Durmaz, Haluk Akin, Huseyin Onay, et al.Biomed Research International|April 16, 2015
Evolution of genetic techniques: past, present, and beyondAsude Alpman Durmaz, Emin Karaca, Urszula Demkow, et al.Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|June 7, 2016
A case of acute lymphoblastic leukemia with additional chromosomes X and 5 associated with a Philadelphia chromosome in the bone marrowBurak Durmaz, Asude Alpman Durmaz, Emin Karaca, et al.Journal of Pediatric Hematology/Oncology|July 29, 2009
A severe alpha thalassemia case compound heterozygous for Hb Adana in alpha1 gene and 20.5 kb double gene deletionAsude Alpman Durmaz, Haluk Akin, Aslihan Yilmaz Ekmekci, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 21, 2021
Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapyGurkan Tarcin, Hande Turan, Aydilek Dagdeviren Cakir, et al.Journal of Genetic Counseling|January 12, 2011
Reasons for adult referrals for genetic counseling at a genetics center in Izmir, Turkey: analysis of 8965 cases over an eleven-year periodOzgur Cogulu, Ferda Ozkinay, Haluk Akin, et al.Pageof 1