6Wang Ying,Zhao Hongshan,Zhang Xiaoxia,et al.Novel identification of a four-base-pair deletion mutation in PITX2 in a Rieger syndrome family[J].J Dent Res,2003,82:1008-1012.
7Ruhin B,Martinot V,Lafforgue P,et al.Pure ectodermal dysplasia:retrospective study of 16 cases and literature review[J].Cleft Palate Craniofac J,2001,38:504-518.
9Tao R,Jin B,Guo SZ,et al.A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia[J].J Hum Genet,2006,51:498-502.
10Gerits A,Nieminen P,de Muynck S,et al.Exclusion of coding region mutations in MSX1,PAX9 and AXIN2 in eight patients with severe oligodontia phenotype[J].Orthod Craniofac Res,2006,9:129-316.