A rare Koolen de Vries syndrome caused by 17q21.31 deletion that encompassing KANSL1 gene

Akcan M. B., Kaya D., Sönmez V., Kablan A., Özdemir Ö., Sılan F.

13th European Cytogenomics Conferece, Bari, Italy, 3 - 05 July 2021, pp.0-1

  • Publication Type: Conference Paper / Summary Text
  • City: Bari
  • Country: Italy
  • Page Numbers: pp.0-1
  • Çanakkale Onsekiz Mart University Affiliated: Yes