Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/5003
Title: Apert syndrome
Authors: Kılıç, İlknur.
Baykara, Y.
Semerci, Cavidan Nur.
Ergin, Hacer.
Tufan Şatıroğlu, N. Lale
Keywords: Apert syndrome
FGFR2 mutation
fibroblast growth factor receptor 2
acrocephalosyndactyly
article
case report
craniofacial synostosis
face malformation
gene mutation
genetic analysis
heart atrium septum defect
human
male
newborn
syndactyly
Turkey (republic)
Abstract: Abstract Not Available
URI: https://hdl.handle.net/11499/5003
ISSN: 1300-0144
Appears in Collections:Tıp Fakültesi Koleksiyonu
TR Dizin İndeksli Yayınlar Koleksiyonu / TR Dizin Indexed Publications Collection

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