Identification of a novel missence mutation in FGFR3 gene in an Iranian family with LADD syndrome by Next-Generation Sequencing
| Autor: | Talebi, Farah, Ghanbari Mardasi, Farideh, Mohammadi Asl, Javad, Bavarsad, Amir Hooshang, Tizno, Saeed |
|---|---|
| Zdroj: | In International Journal of Pediatric Otorhinolaryngology June 2017 97:192-196 |
| Databáze: | ScienceDirect |
| Externí odkaz: |
|
Full Text from ScienceDirect