Ma X - Search Results

1

[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. Among authors: ma x. 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.

2

[CAG repeats of DNA polymerase gamma in Chinese males and relationship of idiopathic male infertility to CAG repeats].

Yao N, Zheng JF, Peng YF, Li ZX, Peng ZQ, Jin XH, Ma X. Yao N, et al. Among authors: ma x. Zhonghua Nan Ke Xue. 2006 Aug;12(8):681-4, 688. Zhonghua Nan Ke Xue. 2006. PMID: 16970152 Chinese.

3

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: ma x. Mol Vis. 2008 Jan 11;14:56-60. Mol Vis. 2008. PMID: 18246032 Free PMC article.

4

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: ma x. Genet Test. 2007 Winter;11(4):445-9. doi: 10.1089/gte.2007.0035. Genet Test. 2007. PMID: 18294062

5

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: ma x. Mol Vis. 2008 Mar 4;14:378-86. Mol Vis. 2008. PMID: 18334953 Free PMC article.

6

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: ma x. Hum Mutat. 2008 May;29(5):769. doi: 10.1002/humu.20724. Hum Mutat. 2008. PMID: 18407550

7

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: ma x. Mol Vis. 2008 Apr 24;14:750-5. Mol Vis. 2008. PMID: 18449377 Free PMC article.

8

[Sperm mtDNA content and mtDNA4977bp deletion in normal and leukocytospermia men].

Zhou WH, Ma X, Jiang H, Yuan RP, Chen Q, Sui YJ, Jia MC. Zhou WH, et al. Among authors: ma x. Zhonghua Nan Ke Xue. 2008 May;14(5):391-5. Zhonghua Nan Ke Xue. 2008. PMID: 18572854 Chinese.

9

A novel mutation in EXT2 gene in a Chinese family with hereditary multiple exostoses.

Liu SG, Lu DG, Liu ZQ, Liu CY, Zhang AY, Li ZQ, Ma X. Liu SG, et al. Among authors: ma x. Genet Test. 2008 Sep;12(3):331-2. doi: 10.1089/gte.2007.0124. Genet Test. 2008. PMID: 18666861

10

[A novel PAX6 mutation (c.1286delC) in the patients with hereditary congenital aniridia.].

Sun DG, Yang JH, Tong Y, Zhao GJ, Ma X. Sun DG, et al. Among authors: ma x. Yi Chuan. 2008 Oct;30(10):1301-6. doi: 10.3724/sp.j.1005.2008.01301. Yi Chuan. 2008. PMID: 18930890 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

34,930 results

Search Page

Filters