Ma X - Search Results

1

Erectile dysfunction in Fragile X patients.

Gu F, Zhang HY, Hu SY, Huang SZ, Ma X, Zhang YQ. Gu F, et al. Among authors: ma x. Asian J Androl. 2006 Jul;8(4):483-7. doi: 10.1111/j.1745-7262.2006.00156.x. Asian J Androl. 2006. PMID: 16763726 Free article.

2

A differentially methylated region of the DAZ1 gene in spermatic and somatic cells.

Li ZX, Ma X, Wang ZH. Li ZX, et al. Among authors: ma x. Asian J Androl. 2006 Jan;8(1):61-7. doi: 10.1111/j.1745-7262.2006.00069.x. Asian J Androl. 2006. PMID: 16372120 Free article.

3

A missense mutation in the gammaD-crystallin gene CRYGD associated with autosomal dominant congenital cataract in a Chinese family.

Gu F, Li R, Ma XX, Shi LS, Huang SZ, Ma X. Gu F, et al. Among authors: ma xx, ma x. Mol Vis. 2006 Jan 10;12:26-31. Mol Vis. 2006. PMID: 16446699 Free article.

4

[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.

5

A novel COL1A1 nonsense mutation causing osteogenesis imperfecta in a Chinese family.

Liu W, Gu F, Ji J, Lu D, Li X, Ma X. Liu W, et al. Among authors: ma x. Mol Vis. 2007 Mar 9;13:360-5. Mol Vis. 2007. PMID: 17392686 Free PMC article.

6

A missense mutation S228P in the CRYBB1 gene causes autosomal dominant congenital cataract.

Wang J, Ma X, Gu F, Liu NP, Hao XL, Wang KJ, Wang NL, Zhu SQ. Wang J, et al. Among authors: ma x. Chin Med J (Engl). 2007 May 5;120(9):820-4. Chin Med J (Engl). 2007. PMID: 17531125

7

A novel mutation in major intrinsic protein of the lens gene (MIP) underlies autosomal dominant cataract in a Chinese family.

Gu F, Zhai H, Li D, Zhao L, Li C, Huang S, Ma X. Gu F, et al. Among authors: ma x. Mol Vis. 2007 Sep 11;13:1651-6. Mol Vis. 2007. PMID: 17893667

8

Identification of a novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa.

Jin ZB, Gu F, Ma X, Nao-i N. Jin ZB, et al. Among authors: ma x. Arch Ophthalmol. 2007 Oct;125(10):1407-12. doi: 10.1001/archopht.125.10.1407. Arch Ophthalmol. 2007. PMID: 17923551

9

Somatic and gonadal mosaicism in X-linked retinitis pigmentosa.

Jin ZB, Gu F, Matsuda H, Yukawa N, Ma X, Nao-i N. Jin ZB, et al. Among authors: ma x. Am J Med Genet A. 2007 Nov 1;143A(21):2544-8. doi: 10.1002/ajmg.a.31984. Am J Med Genet A. 2007. PMID: 17935240

10

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.

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