Zheng D - Search Results

1

[Exclusive gene mapping on retinitis pigmentosa with markers on chromosomes 3 in a Chinese kindred].

Liu Z, Deng H, Xi XH, Xia JH, Pan Q, Dai HP, Yang YJ, Deng HX, Xia K, Zheng D. Liu Z, et al. Among authors: zheng d. Zhonghua Yan Ke Za Zhi. 2003 Apr;39(4):206-8. Zhonghua Yan Ke Za Zhi. 2003. PMID: 12882697 Chinese.

2

A novel PRPF31 splice-site mutation in a Chinese family with autosomal dominant retinitis pigmentosa.

Xia K, Zheng D, Pan Q, Liu Z, Xi X, Hu Z, Deng H, Liu X, Jiang D, Deng H, Xia J. Xia K, et al. Among authors: zheng d. Mol Vis. 2004 May 20;10:361-5. Mol Vis. 2004. PMID: 15162096 Free article.

3

[Splicing site mutation of D19S418 in PRPF-31 gene and its phenotypic characters with autosomal dominant retinitis pigmentosa].

Xi XH, Zheng D, Xia K, Pan Q, Lei LY, Liu Z, Tang CZ, Xia JH, Jiang DY, Deng HX. Xi XH, et al. Among authors: zheng d. Zhonghua Yan Ke Za Zhi. 2005 Nov;41(11):1020-6. Zhonghua Yan Ke Za Zhi. 2005. PMID: 16318756 Chinese.

4

[A simple and convenient method for construction of gene site-directed mutagenesis].

Zhang M, Wen J, Xia K, Zheng D, Zhang Z, Xia J. Zhang M, et al. Among authors: zheng d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Apr;19(2):145-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 11941593 Chinese.

5

A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.

Xia J, Deng H, Feng Y, Zhang H, Pan Q, Dai H, Long Z, Tang B, Deng H, Chen Y, Zhang R, Zheng D, He Y, Xia K. Xia J, et al. Among authors: zheng d. J Hum Genet. 2002;47(12):635-40. doi: 10.1007/s100380200098. J Hum Genet. 2002. PMID: 12522684

6

[Construction of middle fragment deletion mutant with improved gene splicing by overlap extension].

Li CH, Fang HY, Deng XY, Xia K, Zheng D, Xia JH. Li CH, et al. Among authors: zheng d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb;21(1):52-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 14767910 Chinese.

7

[A mutation IVS2+1G>A in EXT2 gene causes hereditary multiple exostoses].

Hu ZM, Zheng D, Pan Q, Yang YF, Zhao TL, Liu XP, Wu LQ, Jiang DG, Xia K, Xia JH. Hu ZM, et al. Among authors: zheng d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Apr;21(2):97-100. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15079787 Chinese.

8

[Silica nanoparticles modified as carriers for gene transfection].

Xue ZG, Zheng D, Ruan JM, Pan Q, Zhao DC, Liu XP, Chen YX, Xia JH, Xia K. Xue ZG, et al. Among authors: zheng d. Yi Chuan Xue Bao. 2003 Jul;30(7):606-10. Yi Chuan Xue Bao. 2003. PMID: 14579527 Chinese.

9

[Genetic diagnosis and prenatal genetic diagnosis of fragile X syndrome].

Wu LQ, Pan Q, Long ZG, Zhu JZ, Dai HP, Zheng D, Xia K, Huang XQ, Xia JH. Wu LQ, et al. Among authors: zheng d. Yi Chuan. 2003 Mar;25(2):123-8. Yi Chuan. 2003. PMID: 15639835 Chinese.

10

A novel MSH2 mutation in a Chinese family with hereditary non-polyposis colorectal cancer.

Zheng D, Li T, Liu X, Hu W, Chen H, Yang Y. Zheng D, et al. Int J Colorectal Dis. 2007 Aug;22(8):875-9. doi: 10.1007/s00384-006-0253-z. Epub 2007 Mar 1. Int J Colorectal Dis. 2007. PMID: 17333219

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