Wang Q - Search Results

1

The G401D mutation of OPA1 causes autosomal dominant optic atrophy and hearing loss in a Chinese family.

Ke T, Nie SW, Yang QB, Liu JP, Zhou LN, Ren X, Liu JY, Wang Q, Liu MG. Ke T, et al. Among authors: wang q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Oct;23(5):481-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 17029191

2

Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects.

Tang ZH, Xia L, Chang W, Li H, Shen F, Liu JY, Wang Q, Liu MG. Tang ZH, et al. Among authors: wang q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Apr;23(2):134-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16604480

3

[Mutation of Thr704Met in SCN 4A causes normoKPP in a Chinese family].

Ren X, Bu BT, Yao Q, Qiu X, Liu JY, Wang Q, Liu MG. Ren X, et al. Among authors: wang q. Yi Chuan. 2006 Aug;28(8):923-6. Yi Chuan. 2006. PMID: 16870577 Chinese.

4

Mutation p.Arg954Trp of KIF21A causes congenital fibrosis of the extraocular muscles in a Chinese family.

Zhang XQ, Peng JH, Tang ZH, Xu CQ, Zhou X, Gong SX, Liu JY, Wang Q, Liu MG. Zhang XQ, et al. Among authors: wang q. Yi Chuan Xue Bao. 2006 Aug;33(8):685-91. doi: 10.1016/S0379-4172(06)60100-5. Yi Chuan Xue Bao. 2006. PMID: 16939002

5

[Genetic analysis of GJB2 in a Chinese family with nonsyndromic hearing impairment].

Zhu QH, Li H, Liu P, Zhu ZF, Wang X, Yuan WL, Liu JY, Mao HY, Wang Q, Liu MG. Zhu QH, et al. Among authors: wang x, wang q. Yi Chuan. 2007 Feb;29(2):172-6. doi: 10.1360/yc-007-0172. Yi Chuan. 2007. PMID: 17369171 Chinese.

6

Ser217Cys mutation in the Ig II domain of FGFR3 in a Chinese family with autosomal dominant achondroplasia.

Zhang SR, Zhou XQ, Ren X, Wang TT, Yuan MX, Wang Q, Liu JY, Liu MG. Zhang SR, et al. Among authors: wang tt, wang q. Chin Med J (Engl). 2007 Jun 5;120(11):1017-9. Chin Med J (Engl). 2007. PMID: 17624273 No abstract available.

7

[NF1 mutation analysis in a Chinese family with neuro- fibromatosis type].

Huang YH, Yang QB, Deng YH, Yu NW, Wang Q, Liu MG. Huang YH, et al. Among authors: wang q. Yi Chuan. 2008 Mar;30(3):309-12. doi: 10.3724/sp.j.1005.2008.00309. Yi Chuan. 2008. PMID: 18331998 Chinese.

8

The R1947X mutation of NF1 causing autosomal dominant neurofibromatosis type 1 in a Chinese family.

Yang Q, Huang C, Yang X, Feng Y, Wang Q, Liu M. Yang Q, et al. Among authors: wang q. J Genet Genomics. 2008 Feb;35(2):73-6. doi: 10.1016/S1673-8527(08)60011-9. J Genet Genomics. 2008. PMID: 18407053

9

Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family.

Liu P, Li H, Ren X, Mao H, Zhu Q, Zhu Z, Yang R, Yuan W, Liu J, Wang Q, Liu M. Liu P, et al. Among authors: wang q. J Genet Genomics. 2008 Sep;35(9):553-8. doi: 10.1016/S1673-8527(08)60075-2. J Genet Genomics. 2008. PMID: 18804074

10

[Two variants in MYOC and CYP1B1 genes in a Chinese family with primary angle-closure glaucoma].

Dai X, Nie S, Ke T, Liu J, Wang Q, Liu M. Dai X, et al. Among authors: wang q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Oct;25(5):493-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18841557 Chinese.

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