Showing results (1-10 of 81) with videos related to
Sort By:
Pageof 9
American Journal of Medical Genetics. Part A|December 10, 2014
A new patient with LACHT syndrome (Mardini-Nyhan association)Tahir Atik, Huseyin Ozan Torun, Ozgur Cogulu, et al.Mutation Research|December 31, 2002
Valproic acid and lamotrigine treatment during pregnancy. The risk of chromosomal abnormalityFerda Ozkinay, Ozgur Cogulu, Cumhur Gunduz, et al.Clinical Dysmorphology|March 14, 2007
Two cases of macrocephaly and immune deficiencyOzgur Cogulu, Ayca Aykut, Necil Kutukculer, et al.European Journal of Medical Genetics|September 24, 2018
Biallelic TOR1A mutations cause severe arthrogryposis: A case requiring reverse phenotypingEsra Isik, Ayca Aykut, Tahir Atik, et al.Molecular Biology Reports|May 19, 2009
MEFV mutations in patients with Familial Mediterranean Fever from the Aegean region of TurkeyHaluk Akin, Huseyin Onay, Emre Turker, et al.Journal of Tropical Pediatrics|January 11, 2014
A new mutation in the TBX5 gene in Holt-Oram syndrome: two cases in the same family and prenatal diagnosisTahir Atik, Huseyin Dervisoglu, Huseyin Onay, et al.Leukemia Research|March 28, 2006
Unusual course of an acute lymphoblastic leukemia case with i(9q) as a sole cytogenetic abnormalityOzgur Cogulu, Deniz Yilmaz Karapinar, Emin Karaca, et al.The Journal of Clinical Endocrinology and Metabolism|July 7, 2005
A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasiaAbhimanyu Garg, Ozgur Cogulu, Ferda Ozkinay, et al.Developmental Medicine and Child Neurology|May 17, 2005
Ring chromosome 20 syndrome with intractable epilepsyAsude Alpman, Gul Serdaroglu, Ozgur Cogulu, et al.Clinical Neurology and Neurosurgery|July 1, 2018
Clinical and genetic features of L1 syndrome patients: Definition of two novel mutationsEsra Isik, Huseyin Onay, Tahir Atik, et al.Pageof 9