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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.Pediatrics International : Official Journal of the Japan Pediatric Society|October 3, 2003
Evaluation of 80 children with prolonged feverOzgur Cogulu, Guldane Koturoglu, Zafer Kurugol, et al.Hormone Research in Paediatrics|October 27, 2010
Gonadotropin-dependent precocious puberty in a patient with X-linked adrenal hypoplasia congenita caused by a novel DAX-1 mutationSukran Darcan, Damla Goksen, Samim Ozen, et al.The Turkish Journal of Pediatrics|July 20, 2006
Pyoderma gangrenosum in a six-month-old boyGüldane Koturoğlu, Fadil Vardar, Ferda Ozkinay, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2013
Analysis of the β-glucocerebrosidase gene in Turkish Gaucher disease patients: mutation profile and description of a novel mutant alleleEmin Karaca, Sema Kalkan, Huseyin Onay, et al.Clinical Dysmorphology|June 7, 2007
Seckel syndrome with Morgagni herniaAsan Onder, Ozgur Cogulu, Aslihan Ekmekci, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2004
HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome presenting with hypocalcemia-induced generalized psoriasisSerap Aksoylar, Yeşim Aydinok, Erkin Serdaroğlu, et al.Gene|July 8, 2015
Two novel UBR1 gene mutations ın a patient with Johanson Blizzard Syndrome: A mild phenotype without mental retardationTahir Atik, Miray Karakoyun, Maja Sukalo, et al.Allergy and Asthma Proceedings|October 18, 2008
Association of interleukin-1beta and interleukin-1 receptor antagonist gene polymorphisms in Turkish children with atopic asthmaDost Zeyrek, Esen Demir, Asude Alpman, et al.Developmental Medicine and Child Neurology|May 17, 2005
Ring chromosome 20 syndrome with intractable epilepsyAsude Alpman, Gul Serdaroglu, Ozgur Cogulu, et al.Pageof 15