Wong L-JC, Chen T-J, Dai P, Bird L, Muenke M. 2001. Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndrome. Am J Med Genet 102:282-285

• Publisher: John Wiley and Sons
• Year: 2002
• Tongue: English
• Weight: 18 KB
• Volume: 109
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/ajmg.10390