Zhang M - Search Results

1

Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts.

Li F, Wang S, Gao C, Liu S, Zhao B, Zhang M, Huang S, Zhu S, Ma X. Li F, et al. Among authors: zhang m. Mol Vis. 2008 Mar 4;14:378-86. Mol Vis. 2008. PMID: 18334953 Free PMC article.

2

A novel mutation in FRMD7 causing X-linked idiopathic congenital nystagmus in a large family.

He X, Gu F, Wang Y, Yan J, Zhang M, Huang S, Ma X. He X, et al. Among authors: zhang m. Mol Vis. 2008 Jan 11;14:56-60. Mol Vis. 2008. PMID: 18246032 Free PMC article.

3

A novel mutation in AlphaA-crystallin (CRYAA) caused autosomal dominant congenital cataract in a large Chinese family.

Gu F, Luo W, Li X, Wang Z, Lu S, Zhang M, Zhao B, Zhu S, Feng S, Yan YB, Huang S, Ma X. Gu F, et al. Among authors: zhang m. Hum Mutat. 2008 May;29(5):769. doi: 10.1002/humu.20724. Hum Mutat. 2008. PMID: 18407550

4

Nonsense mutation in the CRYBB2 gene causing autosomal dominant progressive polymorphic congenital coronary cataracts.

Li FF, Zhu SQ, Wang SZ, Gao C, Huang SZ, Zhang M, Ma X. Li FF, et al. Among authors: zhang m. Mol Vis. 2008 Apr 24;14:750-5. Mol Vis. 2008. PMID: 18449377 Free PMC article.

5

A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts.

Ma X, Li FF, Wang SZ, Gao C, Zhang M, Zhu SQ. Ma X, et al. Among authors: zhang m. Mol Vis. 2008;14:1906-11. Epub 2008 Oct 24. Mol Vis. 2008. PMID: 18958306 Free PMC article.

6

Autosomal dominant congenital nuclear cataracts caused by a CRYAA gene mutation.

Li FF, Yang M, Ma X, Zhang Q, Zhang M, Wang SZ, Zhu SQ. Li FF, et al. Among authors: zhang m, zhang q. Curr Eye Res. 2010 Jun;35(6):492-8. doi: 10.3109/02713681003624901. Curr Eye Res. 2010. PMID: 20465443

7

A novel mutation in the connexin 50 gene (GJA8) associated with autosomal dominant congenital nuclear cataract in a Chinese family.

Gao X, Cheng J, Lu C, Li X, Li F, Liu C, Zhang M, Zhu S, Ma X. Gao X, et al. Among authors: zhang m. Curr Eye Res. 2010 Jul;35(7):597-604. doi: 10.3109/02713681003725831. Curr Eye Res. 2010. PMID: 20597646

8

[EXT1 and EXT2 mutation identified by denaturing high performance liquid chromatograph in three families with hereditary multiple exostoses].

Zhang M, Liu SG, Li FF, Zhou WH, Jin XH, Ma X. Zhang M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Dec;24(6):646-51. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 18067075 Chinese.

9

A novel mutation in the EXT2 gene identified in two unrelated Chinese families with hereditary multiple exostoses.

Liu SG, Li FF, Huang SZ, Chen Y, Wang J, Lu DG, Zhang M, Ma X. Liu SG, et al. Among authors: zhang m. Genet Test. 2007 Winter;11(4):445-9. doi: 10.1089/gte.2007.0035. Genet Test. 2007. PMID: 18294062

10

A novel frameshift mutation in FRMD7 causing X-linked idiopathic congenital nystagmus.

He X, Gu F, Wang Z, Wang C, Tong Y, Wang Y, Yang J, Liu W, Zhang M, Ma X. He X, et al. Among authors: zhang m. Genet Test. 2008 Dec;12(4):607-13. doi: 10.1089/gte.2008.0070. Genet Test. 2008. PMID: 19072571

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