Zhang Q - Search Results

1

CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projection.

Ouyang J, Sun W, Xiao X, Li S, Jia X, Zhou L, Wang P, Zhang Q. Ouyang J, et al. Among authors: zhang q. Hum Mol Genet. 2019 Jun 15;28(12):1959-1970. doi: 10.1093/hmg/ddz029. Hum Mol Genet. 2019. PMID: 30689892 Free PMC article.

2

[The SNPs analysis of encoding sequence of interacting factor gene in Chinese population].

Li J, Zhang QJ, Xiao XS, Li JZ, Zhang FS, Li SQ, Li W, Li T, Jia XY, Guo L, Guo XM. Li J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Oct;20(5):454-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 14556208 Chinese.

3

Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.

Li A, Jiao X, Munier FL, Schorderet DF, Yao W, Iwata F, Hayakawa M, Kanai A, Shy Chen M, Alan Lewis R, Heckenlively J, Weleber RG, Traboulsi EI, Zhang Q, Xiao X, Kaiser-Kupfer M, Sergeev YV, Hejtmancik JF. Li A, et al. Among authors: zhang q. Am J Hum Genet. 2004 May;74(5):817-26. doi: 10.1086/383228. Epub 2004 Mar 23. Am J Hum Genet. 2004. PMID: 15042513 Free PMC article.

4

Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.

Zhang Q, Zulfiqar F, Riazuddin SA, Xiao X, Ahmad Z, Riazuddin S, Hejtmancik JF. Zhang Q, et al. Mol Vis. 2004 Nov 17;10:884-9. Mol Vis. 2004. PMID: 15570217 Free article.

5

Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.

Zhang Q, Guo X, Xiao X, Yi J, Jia X, Hejtmancik JF. Zhang Q, et al. Mol Vis. 2004 Nov 17;10:890-900. Mol Vis. 2004. PMID: 15570218 Free article.

6

[Variations of the zinc finger protein 161 gene in Chinese with or without high myopia].

Wang GB, Zhang QJ, Xiao XS, Li JZ, Zhang FS, Li SQ, Li W, Li T, Jia XY, Guo L, Guo XM. Wang GB, et al. Yi Chuan. 2004 Mar;26(2):155-9. Yi Chuan. 2004. PMID: 15639979 Chinese.

7

[Analysis of GUCA1B,GNGT1 and RGS9 genes in patients with retinitis pigmentosa].

Zhang QJ, Li W, Xiao XS, Li SQ, Guo XM. Zhang QJ, et al. Yi Chuan. 2002 Jan;24(1):19-21. Yi Chuan. 2002. PMID: 15901556 Chinese.

8

[Clinical features and the mutation of Leber's hereditary optic neuropathy in Chinese patients].

Wang Y, Guo XM, Jia XY, Li SQ, Xiao XS, Guo L, Zhang QJ. Wang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):334-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952130 Chinese.

9

A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.

Zhang Q, Guo X, Xiao X, Jia X, Li S, Hejtmancik JF. Zhang Q, et al. Mol Vis. 2005 Jul 22;11:554-60. Mol Vis. 2005. PMID: 16052171 Free article.

10

[Variation of the peripherin gene in Chinese with or without high myopia].

Li J, Zhang QJ, Fu R, Xiao XS, Li JZ, Zhang FS, Li SQ, Li W, Li T, Jia XY, Guo L, Guo XM. Li J, et al. Yi Chuan. 2002 Sep;24(5):523-6. Yi Chuan. 2002. PMID: 16135441 Chinese.

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