Improved diagnosis of a common mutation (R248C) in the human growth factor receptor 3 (FGFR3) gene that causes type I Thanatophoric dysplasia

✍ Scribed by Mehmet Simsek; Lihadh Al-Gazali; Reyhanah Al-Mjeni; Riad Bayoumi

• Book ID: 108313609
• Publisher: Elsevier Science
• Year: 2003
• Tongue: English
• Weight: 62 KB
• Volume: 36
• Category: Article
• ISSN: 0009-9120
• DOI: 10.1016/s0009-9120(02)00441-1