A case report of Xp21 contiguous gene syndrome adrenal hypoplasia congenita Glycerol kinase deficiency and Duchenne muscular dystrophy | AVESİS

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A case report of Xp21 contiguous gene syndrome adrenal hypoplasia congenita Glycerol kinase deficiency and Duchenne muscular dystrophy

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KARA C., YILMAZ G. C., ÇELEBİ BİTKİN E., AYDIN H. M.

PES (Current Trends in Pediatric Endocrinology A PES Perspective), İstanbul, Turkey, 13 - 14 May 2016

Publication Type: Conference Paper / Summary Text
City: İstanbul
Country: Turkey
Ondokuz Mayıs University Affiliated: Yes