Wei L - Search Results

1

[Mutation analysis of NF2 gene and clinical investigation in a Chinese family with neurofibromatosis type II].

Cui YX, Xia XY, Huang TT, Wei L, Fan XB, Yao B, Ge YF, Li XJ, Huang YF. Cui YX, et al. Among authors: wei l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Dec;27(6):688-91. doi: 10.3760/cma.j.issn.1003-9406.2010.06.020. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 21154335 Chinese.

2

A novel insertion mutation in the SEDL gene results in X-linked spondyloepiphyseal dysplasia tarda in a large Chinese pedigree.

Xia XY, Cui YX, Zhou YC, Zhou X, Shi YC, Wei L, Li XJ, Huang YF, Huang TT. Xia XY, et al. Among authors: wei l. Clin Chim Acta. 2009 Dec;410(1-2):39-42. doi: 10.1016/j.cca.2009.09.016. Epub 2009 Sep 19. Clin Chim Acta. 2009. PMID: 19766614

3

[Mutation of the USP26 gene in spermatogenesis dysfunction].

Wei L, Shi YC, Cui YX, Huang YF. Wei L, et al. Zhonghua Nan Ke Xue. 2010 Jan;16(1):65-7. Zhonghua Nan Ke Xue. 2010. PMID: 20180409 Review. Chinese.

4

[AZF microdeletions on the Y chromosome in infertile Chinese men: a five-year retrospective analysis].

Shi YC, Cui YX, Wei L, Zhou YC, Shao Y, Xia XY, Shang XJ, Zhu WM, Huang YF. Shi YC, et al. Among authors: wei l. Zhonghua Nan Ke Xue. 2010 Apr;16(4):314-9. Zhonghua Nan Ke Xue. 2010. PMID: 20626158 Chinese.

5

[Sex chromosomes and male infertility].

Shi YC, Wei L, Cui YX, Huang YF. Shi YC, et al. Among authors: wei l. Zhonghua Nan Ke Xue. 2010 May;16(5):460-7. Zhonghua Nan Ke Xue. 2010. PMID: 20684331 Review. Chinese.

6

Association between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men.

Shi YC, Wei L, Cui YX, Shang XJ, Wang HY, Xia XY, Zhou YC, Li H, Jiang HT, Zhu WM, Huang YF. Shi YC, et al. Among authors: wei l. Clin Chim Acta. 2011 Mar 18;412(7-8):545-9. doi: 10.1016/j.cca.2010.12.005. Epub 2010 Dec 10. Clin Chim Acta. 2011. PMID: 21147082

7

A G560S mutation in alpha1 (I) collagen causes familial osteogenesis imperfecta type IV.

Cui YX, Xia XY, Shi YC, Wei L, Liang Q, Yao B, Ge YF, Huang YF, Li XJ. Cui YX, et al. Among authors: wei l. Clin Chim Acta. 2009 Nov;409(1-2):145-6. doi: 10.1016/j.cca.2009.09.008. Epub 2009 Sep 12. Clin Chim Acta. 2009. PMID: 19751715 No abstract available.

8

A rare Y chromosome constitutional rearrangement: a partial AZFb deletion and duplication within chromosome Yp in an infertile man with severe oligoasthenoteratozoospermia.

Shi YC, Cui YX, Zhou YC, Wei L, Jiang HT, Xia XY, Lu HY, Wang HY, Shang XJ, Zhu WM, Li XJ, Huang YF. Shi YC, et al. Among authors: wei l. Int J Androl. 2011 Oct;34(5 Pt 1):461-9. doi: 10.1111/j.1365-2605.2010.01098.x. Int J Androl. 2011. PMID: 21950337

9

Meiotic pairing error in an infertile male bearing reciprocal deletion of chromosome 13.

Cui YX, Wei L, Xia XY, Fan XB, Shi YC, Yao B, Ge YF, Li XJ, Huang YF. Cui YX, et al. Among authors: wei l. J Androl. 2011 Sep-Oct;32(5):473-7. doi: 10.2164/jandrol.109.009738. Epub 2010 Dec 16. J Androl. 2011. PMID: 21164148

10

Synthesis of Tc-D,D-HMPAO and Tc-L,L-HMPAO and their comparison of chemical and biological properties.

Ding HJ, Huang YF, Tzeng CC, Wei LM, Yeh SJ. Ding HJ, et al. Among authors: wei lm. Bioorg Med Chem Lett. 1999 Nov 15;9(22):3199-202. doi: 10.1016/s0960-894x(99)00557-0. Bioorg Med Chem Lett. 1999. PMID: 10576687

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