A Case Report of Xp21 Contiguous Gene Syndrome: Adrenal Hypoplasia Congenita, Glycerol Kinase Deficiency, and Duchenne Muscular Dystrophy - Kara, Cengiz; Yilmaz, Gulay Can; Bitkin, Eda Celebi; Aydin, Murat (Journal of clinical research in pediatric endocrinology, 2016)
Keywords: Case studies; Diagnosis; Genetic aspects; Neonatal diseases