|1.||Wu, Xiaoming: 1 article (12/2014)|
|2.||Xiao, Jingjing: 1 article (12/2014)|
|3.||Wu, Renhua: 1 article (12/2014)|
|4.||Sun, Shiying: 1 article (12/2014)|
|5.||Chen, Peng: 1 article (12/2014)|
|6.||Wang, Ye: 1 article (12/2014)|
|7.||Zhao, Xiaowen: 1 article (12/2014)|
|8.||Guan, Liping: 1 article (12/2014)|
|9.||Dai, Yunhai: 1 article (12/2014)|
|10.||Zhang, Qingyan: 1 article (12/2014)|
01/01/2006 - "This study provides the report of mapping a locus for syndromal cataract (cataract-microcornea syndrome) on 21q22.3. The mutation observed in CRYAA in the present family highlights the phenotypic heterogeneity of the disorder in relation to the genotype, as an identical mutation has previously been reported in an American family with a different type of cataract. "
12/01/2014 - "Cataract-microcornea syndrome (CCMC) is an autosomal dominant inherited disease characterized by the association of congenital cataract and microcornea without any other systemic anomaly or dysmorphism. "
03/01/2011 - "Congenital cataract-microcornea syndrome (CCMC) is a clinically and genetically heterogeneous condition characterized by lens opacities and microcornea. "
01/01/2007 - "One novel mutation affecting a known cataract gene was identified among four unrelated individuals with presumed autosomal dominant congenital cataract-microcornea syndrome. "