Related Articles
C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients
Detection of G338R FGFR2 mutation in a Vietnamese patient with Crouzon syndrome
Bestrophin 1 gene analysis and associated clinical findings in a Chinese patient with Best vitelliform macular dystrophy
Molecular analysis of FGFR 2 and associated clinical observations in two Chinese families with Crouzon syndrome
Two heterozygous mutations identified in one Chinese patient with bilateral macular coloboma