An infant with X-linked adrenal hypoplasia congenita and Xp21 contiguous gene deletion syndrome.

KARAGÜZEL G., Mutlu M., Çebi A. H., Şahin S., Polat R.

55th annual ESPE (European Society for Paediatric Endocrinology) Meeting, Paris, France, 10 - 12 September 2016, pp.1, (Full Text)

  • Publication Type: Conference Paper / Full Text
  • City: Paris
  • Country: France
  • Page Numbers: pp.1
  • Karadeniz Technical University Affiliated: Yes