Two different de novo mutations causing syndromic developmental delay in two patients from a consanguineous Turkish family

Castilla-Vallmanya L., Acar S., Giray-Bozkaya O., Prat A., Centeno M., Carbonell-Roque A., ...Daha Fazla

EUROPEAN JOURNAL OF HUMAN GENETICS, cilt.28, ss.462, 2020 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Özet
  • Cilt numarası: 28
  • Basım Tarihi: 2020
  • Dergi Adı: EUROPEAN JOURNAL OF HUMAN GENETICS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, CAB Abstracts, EMBASE, MEDLINE, Veterinary Science Database
  • Sayfa Sayıları: ss.462
  • Dokuz Eylül Üniversitesi Adresli: Evet