Association of developmental delay, congenital adrenal hypoplasia, duchenne muscular dystrophy and glycerol kinase deficiency: a rare Xp21 contiguous gene deletion syndrome

ALTUNDAĞ E., KARA C., SANRI A., MUTLU ALBAYRAK H., YALÇIN H. Y., OĞUR M. G.

Erciyes Medical Genetics Days 2017, 11 - 13 May 2017, vol.39, pp.5000

  • Publication Type: Conference Paper / Summary Text
  • Volume: 39
  • Page Numbers: pp.5000
  • Ondokuz Mayıs University Affiliated: Yes