An infant with two de novo variants causing recessive and dominant disorders: Diagnostic challenge


Sezer A. , Ogutlu O. B. G. , TÜRKYILMAZ Z. , GÜCÜYENER K. , KAYHAN G. , PERÇİN F. E.

EUROPEAN JOURNAL OF HUMAN GENETICS, vol.28, pp.895, 2020 (Journal Indexed in SCI) identifier

  • Publication Type: Article / Abstract
  • Volume: 28
  • Publication Date: 2020
  • Title of Journal : EUROPEAN JOURNAL OF HUMAN GENETICS
  • Page Numbers: pp.895