Wang QK - Search Results

1

Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification.

Dai X, Gao Y, Xu Z, Cui X, Liu J, Li Y, Xu H, Liu M, Wang QK, Liu JY. Dai X, et al. Among authors: wang qk. Am J Med Genet B Neuropsychiatr Genet. 2010 Oct 5;153B(7):1305-10. doi: 10.1002/ajmg.b.31102. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20552677

2

A novel heterozygous mutation in the Indian hedgehog gene (IHH) is associated with brachydactyly type A1 in a Chinese family.

Liu M, Wang X, Cai Z, Tang Z, Cao K, Liang B, Ren X, Liu JY, Wang QK. Liu M, et al. Among authors: wang x, wang qk. J Hum Genet. 2006;51(8):727-731. doi: 10.1007/s10038-006-0012-6. Epub 2006 Jul 27. J Hum Genet. 2006. PMID: 16871364

3

Novel HSF4 mutation causes congenital total white cataract in a Chinese family.

Ke T, Wang QK, Ji B, Wang X, Liu P, Zhang X, Tang Z, Ren X, Liu M. Ke T, et al. Among authors: wang x, wang qk. Am J Ophthalmol. 2006 Aug;142(2):298-303. doi: 10.1016/j.ajo.2006.03.056. Am J Ophthalmol. 2006. PMID: 16876512

4

Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family.

Liu M, Ke T, Wang Z, Yang Q, Chang W, Jiang F, Tang Z, Li H, Ren X, Wang X, Wang T, Li Q, Yang J, Liu J, Wang QK. Liu M, et al. Among authors: wang x, wang z, wang t, wang qk. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3461-6. doi: 10.1167/iovs.05-1438. Invest Ophthalmol Vis Sci. 2006. PMID: 16877416

5

A novel mutation in GDF5 causes autosomal dominant symphalangism in two Chinese families.

Wang X, Xiao F, Yang Q, Liang B, Tang Z, Jiang L, Zhu Q, Chang W, Jiang J, Jiang C, Ren X, Liu JY, Wang QK, Liu M. Wang X, et al. Among authors: wang qk. Am J Med Genet A. 2006 Sep 1;140A(17):1846-53. doi: 10.1002/ajmg.a.31372. Am J Med Genet A. 2006. PMID: 16892395

6

A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia.

Huang C, Yang Q, Ke T, Wang H, Wang X, Shen J, Tu X, Tian J, Liu JY, Wang QK, Liu M. Huang C, et al. Among authors: wang h, wang x, wang qk. J Hum Genet. 2006;51(12):1133-1137. doi: 10.1007/s10038-006-0071-8. Epub 2006 Oct 26. J Hum Genet. 2006. PMID: 17066260

7

Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation.

Liu JY, Ren X, Yang X, Guo T, Yao Q, Li L, Dai X, Zhang M, Wang L, Liu M, Wang QK. Liu JY, et al. Among authors: wang l, wang qk. J Hum Genet. 2007;52(6):565-570. doi: 10.1007/s10038-007-0152-3. Epub 2007 May 22. J Hum Genet. 2007. PMID: 17516023

8

A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family.

Zhang X, Chen L, Liu J, Zhao Z, Qu E, Wang X, Chang W, Xu C, Wang QK, Liu M. Zhang X, et al. Among authors: wang x, wang qk. BMC Med Genet. 2007 Aug 8;8:52. doi: 10.1186/1471-2350-8-52. BMC Med Genet. 2007. PMID: 17686168 Free PMC article.

9

A novel de novo frameshift mutation of RPGR ORF15 is associated with X-linked retinitis pigmentosa in a Chinese family.

Chang W, Ding Q, Tang Z, Liu P, Jiang F, Ke T, Ren X, Wang Z, Liu J, Wang QK, Liu M. Chang W, et al. Among authors: wang z, wang qk. Mol Vis. 2007 Aug 30;13:1548-54. Mol Vis. 2007. PMID: 17893654

10

Identification of a genetic locus for ichthyosis vulgaris on chromosome 10q22.3-q24.2.

Liu P, Yang Q, Wang X, Feng A, Yang T, Yang R, Wang P, Yuang M, Liu M, Liu JY, Wang QK. Liu P, et al. Among authors: wang x, wang p, wang qk. J Invest Dermatol. 2008 Jun;128(6):1418-22. doi: 10.1038/sj.jid.5701191. Epub 2007 Dec 13. J Invest Dermatol. 2008. PMID: 18079749 Free article.

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