Trp290Cys mutation in exon IIIa of the fibroblast growth factor receptor 2 (FGFR2) gene is associated with Pfeiffer syndrome

✍ Scribed by Marco Tartaglia; Sonia Valeri; Francesco Velardi; Concezio Di Rocco; P. A. Battaglia

• Publisher: Springer
• Year: 1997
• Tongue: English
• Weight: 157 KB
• Volume: 99
• Category: Article
• ISSN: 0340-6717
• DOI: 10.1007/s004390050413