A case of Weaver Syndrome caused by a novel frameshift EZH2 mutation


TÜRKYILMAZ A., KARAKAYA T., ŞİMŞEK H., SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , ARMAN A. , ...More

European Society of Human Genetics, 21 - 24 May 2016

  • Publication Type: Conference Paper / Full Text