Liu Z - Search Results

1

Confirmation and refinement of a genetic locus of congenital motor nystagmus in Xq26.3-q27.1 in a Chinese family.

Zhang B, Xia K, Ding M, Liang D, Liu Z, Pan Q, Hu Z, Wu LQ, Cai F, Xia J. Zhang B, et al. Among authors: liu z. Hum Genet. 2005 Jan;116(1-2):128-31. doi: 10.1007/s00439-004-1188-5. Epub 2004 Oct 23. Hum Genet. 2005. PMID: 15517395

2

[Insulin resistance in epileptic patients during treatment of valproic acid].

Ding MP, Bao YY, Chen Z, Liu ZR, Xu LL. Ding MP, et al. Among authors: liu zr. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2004 May;33(3):216-8. doi: 10.3785/j.issn.1008-9292.2004.03.009. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2004. PMID: 15179681 Chinese.

3

[Mutation analysis of keratin 9 gene in a pedigree with epidermolytic palmoplantar keratoderma].

Zhang BR, Yin XZ, Xia K, Ding MP, Hu ZM, Zheng M, Liu ZR, Xia JH. Zhang BR, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):570-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583984 Chinese.

4

[Mapping of a pedigree with congenital nystagmus].

Liu ZR, Zhang BR, Ding MP, Xia K, Hu ZM, Deng H, Xia JH. Liu ZR, et al. Yi Chuan. 2004 Jul;26(4):437-40. Yi Chuan. 2004. PMID: 15640035 Chinese.

5

Novel mutations of the FRMD7 gene in X-linked congenital motor nystagmus.

Zhang B, Liu Z, Zhao G, Xie X, Yin X, Hu Z, Xu S, Li Q, Song F, Tian J, Luo W, Ding M, Yin J, Xia K, Xia J. Zhang B, et al. Among authors: liu z. Mol Vis. 2007 Sep 13;13:1674-9. Mol Vis. 2007. PMID: 17893669

6

Novel human pathological mutations. Gene symbol: FRMD7. Disease: congenital motor nystagmus.

Zhang B, Liu Z, Zhao G. Zhang B, et al. Among authors: liu z. Hum Genet. 2007 Nov;122(3-4):414. Hum Genet. 2007. PMID: 18350647 No abstract available.

7

Novel human pathological mutations. Gene symbol: FRMD7. Disease: congenital motor nystagmus.

Zhang B, Liu Z, Zhao G. Zhang B, et al. Among authors: liu z. Hum Genet. 2007 Nov;122(3-4):414. Hum Genet. 2007. PMID: 18350648 No abstract available.

8

Gene symbol: PEO1. Disease: Progressive external ophthalmoplegia.

Liu Z, Ding M. Liu Z, et al. Hum Genet. 2008 Feb;123(1):109. Hum Genet. 2008. PMID: 18386344 No abstract available.

9

[Clinical and genetic analysis of a pedigree of myotonic dystrophy disease].

Ding Y, Ding MP, Yin HM, Guo Y, Zhang J, Zhao GH, Wang J, Liu ZR. Ding Y, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2008 Sep;37(5):494-8. doi: 10.3785/j.issn.1008-9292.2008.05.013. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2008. PMID: 18925718 Chinese.

10

A novel Twinkle (PEO1) gene mutation in a Chinese family with adPEO.

Liu Z, Ding Y, Du A, Zhang B, Zhao G, Ding M. Liu Z, et al. Mol Vis. 2008;14:1995-2001. Epub 2008 Nov 3. Mol Vis. 2008. PMID: 18989381 Free PMC article.

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