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European Journal of Pediatrics|March 26, 2003
Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in TurkeyM Tekin, T Duman, G Boğoçlu, et al.
Clinical Genetics|December 25, 2004
Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in AnatoliaM Tekin, G Boğoclu, S T Arican, et al.
Human Mutation|December 29, 1999
MEFV mutations in Turkish patients suffering from Familial Mediterranean FeverN Akar, M Misiroglu, F Yalcinkaya, et al.
Clinical Genetics|July 19, 2002
657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish familyMustafa Tekin, F Doğu, N Taçyíldiz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 11, 2001
Syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six patientsM Berberoğlu, Z Aycan, G Ocal, et al.
Clinical and Experimental Rheumatology|January 5, 2002
Familial Mediterranean fever (FMF)-associated amyloidosis in childhood. Clinical features, course and outcomeN Cakar, F Yalçinkaya, N Ozkaya, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 23, 2006
Plasminogen activator inhibitor-1 (PAI-1) gene polymorphism (-675 4G/5G) associated with obesity and vascular risk in childrenM Berberoğlu, O Evliyaoğlu, P Adiyaman, et al.
Medical and Pediatric Oncology|January 1, 1993
Burkitt's lymphoma between African and American types in Turkish children: clinical, viral (EBV), and molecular studiesA O Cavdar, S Gözdaşoğlu, G Yavuz, et al.
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