Gu J - Search Results

1

[A novel missense mutation in MIP gene resulted in polymorphic cataract].

Lin H, Wang L, Zhou N, Su H, Gu J, Qi Y. Lin H, et al. Among authors: gu j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Feb;25(1):6-10. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18247294 Chinese.

2

[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.

3

[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.

4

[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.

5

[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.

6

[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.

7

[TGFBI gene mutation analysis in a Chinese family with Thiel-Behnke corneal dystrophy].

Qi YH, He HD, Li Y, Wang L, Lin H, Su H, Gu JZ, Huang SZ. Qi YH, et al. Zhonghua Yan Ke Za Zhi. 2007 Aug;43(8):718-21. Zhonghua Yan Ke Za Zhi. 2007. PMID: 18001570 Chinese.

8

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. Among authors: gu j. Hum Genet. 2004 Jan;114(2):192-7. doi: 10.1007/s00439-003-1049-7. Epub 2003 Nov 4. Hum Genet. 2004. PMID: 14598164

9

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. Mol Vis. 2005 Nov 9;11:971-6. Mol Vis. 2005. PMID: 16288201 Free article.

10

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: gu j. Mol Vis. 2007 Aug 1;13:1357-62. Mol Vis. 2007. PMID: 17768382

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