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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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