Qi Y - Search Results

1

Autosomal-dominant cerulean cataract in a chinese family associated with gene conversion mutation in beta-B2-crystallin.

Wang L, Lin H, Gu J, Su H, Huang S, Qi Y. Wang L, et al. Among authors: qi y. Ophthalmic Res. 2009;41(3):148-53. doi: 10.1159/000209668. Epub 2009 Mar 26. Ophthalmic Res. 2009. PMID: 19321936

2

A deletion mutation in the betaA1/A3 crystallin gene ( CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family.

Qi Y, Jia H, Huang S, Lin H, Gu J, Su H, Zhang T, Gao Y, Qu L, Li D, Li Y. Qi Y, et al. Hum Genet. 2004 Jan;114(2):192-7. doi: 10.1007/s00439-003-1049-7. Epub 2003 Nov 4. Hum Genet. 2004. PMID: 14598164

3

[Autosomal dominant congenital nuclear cataract caused by a deletion mutation in the beta A1-crystallin gene].

Qi YH, Jia HY, Huang SZ, Lin H, Gu JZ, Su H, Zhang TY, Gao Y. Qi YH, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Dec;20(6):486-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 14669215 Chinese.

4

[Gene mapping of a pedigree with autosomal dominant congenital cataract].

Qi YH, Jia HY, Huang SZ, Lin H, Gu JZ, Su H, Zhang TY, Gao Y. Qi YH, et al. Zhonghua Yan Ke Za Zhi. 2004 Dec;40(12):824-7. Zhonghua Yan Ke Za Zhi. 2004. PMID: 15733435 Chinese.

5

A new congenital nuclear cataract caused by a missense mutation in the gammaD-crystallin gene (CRYGD) in a Chinese family.

Gu J, Qi Y, Wang L, Wang J, Shi L, Lin H, Li X, Su H, Huang S. Gu J, et al. Among authors: qi y. Mol Vis. 2005 Nov 9;11:971-6. Mol Vis. 2005. PMID: 16288201 Free article.

6

[Mutation analysis of FOXL2 in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome].

Qi YH, Li Y, Lin H, Jia HY, Su H, Gu JZ, Huang SZ, Liu YP. Qi YH, et al. Zhonghua Yan Ke Za Zhi. 2006 May;42(5):409-14. Zhonghua Yan Ke Za Zhi. 2006. PMID: 16762234 Chinese.

7

[A research on TGFBI gene mutations in Chinese families with corneal dystrophies].

Qi YH, He HD, Li Y, Lin H, Gu JZ, Su H, Huang SZ. Qi YH, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Jun;23(3):310-2. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16767671 Chinese.

8

[Autosomal dominant congenital golden crystal nuclear cataract caused by a missense mutation in gammaD crystallin gene (CRYGD) in a Chinese family].

Gu JZ, Qi YH, Lin H, Li X, Wang J, Meng WM, Su H. Gu JZ, et al. Zhonghua Yan Ke Za Zhi. 2006 Oct;42(10):913-7. Zhonghua Yan Ke Za Zhi. 2006. PMID: 17217786 Chinese.

9

A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.

Wang L, Lin H, Shen Y, Huang S, Gu J, Su H, Qi Y. Wang L, et al. Among authors: qi y. Mol Vis. 2007 Aug 1;13:1357-62. Mol Vis. 2007. PMID: 17768382

10

A substitution of arginine to lysine at the COOH-terminus of MIP caused a different binocular phenotype in a congenital cataract family.

Lin H, Hejtmancik JF, Qi Y. Lin H, et al. Among authors: qi y. Mol Vis. 2007 Sep 30;13:1822-7. Mol Vis. 2007. PMID: 17960133

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