Xu F - Search Results

1

Next-generation sequencing-based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosa.

Fu Q, Wang F, Wang H, Xu F, Zaneveld JE, Ren H, Keser V, Lopez I, Tuan HF, Salvo JS, Wang X, Zhao L, Wang K, Li Y, Koenekoop RK, Chen R, Sui R. Fu Q, et al. Among authors: xu f. Invest Ophthalmol Vis Sci. 2013 Jun 14;54(6):4158-66. doi: 10.1167/iovs.13-11672. Invest Ophthalmol Vis Sci. 2013. PMID: 23661369 Free PMC article.

2

R555W mutation of TGFbetaI related to granular corneal dystrophy in Chinese patients.

Hu L, Xu F, Ma WJ, Zhang H, Sui RF. Hu L, et al. Among authors: xu f. Chin Med J (Engl). 2009 Nov 20;122(22):2691-4. Chin Med J (Engl). 2009. PMID: 19951597

3

Phenotypic expression of X-linked retinoschisis in Chinese families with mutations in the RS1 gene.

Xu F, Xiang H, Jiang R, Dong F, Sui R. Xu F, et al. Doc Ophthalmol. 2011 Aug;123(1):21-7. doi: 10.1007/s10633-011-9278-x. Epub 2011 Jun 24. Doc Ophthalmol. 2011. PMID: 21701876

4

Thirty-two years follow-up of X-linked juvenile retinoschisis in a Chinese patient with RS1 mutation.

Xu F, Sui R, Dong F. Xu F, et al. Ophthalmic Genet. 2012 Jun;33(2):77-82. doi: 10.3109/13816810.2011.628359. Epub 2011 Dec 15. Ophthalmic Genet. 2012. PMID: 22171610

5

Genetic and phenotypic characteristics of three Mainland Chinese families with choroideremia.

Zhou Q, Liu L, Xu F, Li H, Sergeev Y, Dong F, Jiang R, MacDonald I, Sui R. Zhou Q, et al. Among authors: xu f. Mol Vis. 2012;18:309-16. Epub 2012 Feb 3. Mol Vis. 2012. PMID: 22355242 Free PMC article.

6

Novel RPE65 mutations associated with Leber congenital amaurosis in Chinese patients.

Xu F, Dong Q, Liu L, Li H, Liang X, Jiang R, Sui R, Dong F. Xu F, et al. Mol Vis. 2012;18:744-50. Epub 2012 Mar 28. Mol Vis. 2012. PMID: 22509104 Free PMC article.

7

A novel splice site mutation in the COL4A5 gene in a Chinese female patient with rare ocular abnormalities.

Zhao C, Wang F, Zhang Y, Wen Y, Su Y, Zhang C, Sui R, Xu F, Ding J, Dong F. Zhao C, et al. Among authors: xu f. Mol Vis. 2012;18:2205-12. Epub 2012 Aug 8. Mol Vis. 2012. PMID: 22919268 Free PMC article.

8

Novel PRPF31 mutations associated with Chinese autosomal dominant retinitis pigmentosa patients.

Xu F, Sui R, Liang X, Li H, Jiang R, Dong F. Xu F, et al. Mol Vis. 2012;18:3021-xxx. Epub 2012 Dec 14. Mol Vis. 2012. PMID: 23288994 Free PMC article.

9

[Clinical features of congenital stationary night blindness].

Li H, Liu LY, Xu HY, Xu F, Jiang RX, Sui RF. Li H, et al. Among authors: xu hy, xu f. Zhonghua Yi Xue Za Zhi. 2012 Oct 23;92(39):2756-9. Zhonghua Yi Xue Za Zhi. 2012. PMID: 23290162 Chinese.

10

[Progress in the studies of molecular genetics in Bietti crystalline corneoretinal dystrophy].

Xu F, Sui RF, Dong FT. Xu F, et al. Zhonghua Yan Ke Za Zhi. 2012 Oct;48(10):948-51. Zhonghua Yan Ke Za Zhi. 2012. PMID: 23302251 Review. Chinese.

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