MOLECULAR ANALYSIS OF FGFR1-3, TWIST1, MSX2, POR, FREM1 AND RAB23 GENES IN SYNDROMIC AND NON-SYNDROMIC CRANIOSYNOSTOSIS CASES
Tarih
2019Yazar
Karaman, Birsen
Altunoglu, Umut
Basaran, Seher
Toksoy, Guven
Karaman, Volkan
Uyguner, Zehra Oya
Kayserili Karabey, Hulya
Avci, Sahin
Üst veri
Tüm öğe kaydını gösterÖzet
Objective: Craniosynostosis (CS) associated genes (FGFR1-3, TWIST1, MSX2, POR, FREM1 and RAB23) were investigated in order to determine the mutation rates and establish an effective flow chart for molecular genetic diagnosis for syndromic (SCS) and non-syndromic craniosynostosis (NSCS).
Koleksiyonlar
- Makale [92796]