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

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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, Scopus)

• 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