Novel SNP at the common primer site of exon IIIa ofFGFR2 gene causes error in molecular diagnosis of craniosynostosis syndrome

✍ Scribed by Wong, Lee-Jun C. ;Chen, Tian-Jian ;Dai, Pu ;Bird, Lynne ;Muenke, Maximilian

• Publisher: John Wiley and Sons
• Year: 2001
• Tongue: English
• Weight: 141 KB
• Volume: 102
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/ajmg.1461