Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome

✍ Scribed by Lajeunie, Elisabeth; Heuertz, Solange; El Ghouzzi, Vincent; Martinovic, Jelena; Renier, Dominique; Le Merrer, Martine; Bonaventure, Jacky

• Book ID: 110026562
• Publisher: Nature Publishing Group
• Year: 2006
• Tongue: English
• Weight: 262 KB
• Volume: 14
• Category: Article
• ISSN: 1018-4813
• DOI: 10.1038/sj.ejhg.5201558