Liu MG - 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: liu jp, liu mg, liu jy. 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 mutations of the retinitis pigmentosa GTPase regulator gene in two Chinese families with X-linked retinitis pigmentosa.

Liu L, Chen H, Liu M, Jin L, Wei Y, Wu X, Liu Y, Xhu R, Chai J. Liu L, et al. Chin Med J (Engl). 2002 Jun;115(6):833-6. Chin Med J (Engl). 2002. PMID: 12123547

3

Functional analysis of TBX5 missense mutations associated with Holt-Oram syndrome.

Fan C, Liu M, Wang Q. Fan C, et al. J Biol Chem. 2003 Mar 7;278(10):8780-5. doi: 10.1074/jbc.M208120200. Epub 2002 Dec 23. J Biol Chem. 2003. PMID: 12499378 Free PMC article.

4

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family.

Wang Q, Liu M, Xu C, Tang Z, Liao Y, Du R, Li W, Wu X, Wang X, Liu P, Zhang X, Zhu J, Ren X, Ke T, Wang Q, Yang J. Wang Q, et al. J Mol Med (Berl). 2005 Mar;83(3):203-8. doi: 10.1007/s00109-005-0638-4. Epub 2005 Feb 22. J Mol Med (Berl). 2005. PMID: 15726306 Free PMC article.

5

[Advances in the studies on the molecular and genetic aspects of epilepsy].

Wang X, Wang T, Yuan MX, Liu MG, Wang Q. Wang X, et al. Among authors: liu mg. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005 Jun;27(3):388-93. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005. PMID: 16038283 Review. Chinese.

6

Genetic analysis of a family with 46,XY "female" associated with infertility.

Wang X, Wang XR, Liu MG, Wang Q, Liu JY. Wang X, et al. Among authors: liu mg, liu jy. Yi Chuan Xue Bao. 2006 Jan;33(1):19-25. doi: 10.1016/S0379-4172(06)60003-6. Yi Chuan Xue Bao. 2006. PMID: 16450583

7

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: liu mg, liu jy. 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

8

[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: liu mg, liu jy. Yi Chuan. 2006 Aug;28(8):923-6. Yi Chuan. 2006. PMID: 16870577 Chinese.

9

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. 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

10

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. Am J Ophthalmol. 2006 Aug;142(2):298-303. doi: 10.1016/j.ajo.2006.03.056. Am J Ophthalmol. 2006. PMID: 16876512

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