Wang XZ - Search Results

1

[The same mutation Glu208Lys in the GJB1 gene was detected in 2 families with X-linked Charcot-Marie-Tooth disease].

Song SJ, Song SJ, Yan M, Wang XZ, Zhang YZ, Zou JH, Zhong N. Song SJ, et al. Among authors: wang xz. Yi Chuan. 2007 Jul;29(7):800-4. doi: 10.1360/yc-007-0800. Yi Chuan. 2007. PMID: 17646144 Chinese.

2

Clinical and genetic features of DYT1 and DYT5.

Wang XZ, Zhong N. Wang XZ, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Feb 18;38(1):107-9. Beijing Da Xue Xue Bao Yi Xue Ban. 2006. PMID: 16415980 Free article. Review.

3

Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis.

Han D, Gong Y, Wu H, Zhang X, Yan M, Wang X, Qu H, Feng H, Song S. Han D, et al. Eur J Med Genet. 2008 Nov-Dec;51(6):536-46. doi: 10.1016/j.ejmg.2008.06.002. Epub 2008 Jul 9. Eur J Med Genet. 2008. PMID: 18657636

4

Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations.

Wang X, Wang Z, Yan M, Huang S, Chen TJ, Zhong N. Wang X, et al. Behav Brain Funct. 2008 Apr 29;4:20. doi: 10.1186/1744-9081-4-20. Behav Brain Funct. 2008. PMID: 18445268 Free PMC article.

5

Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A.

Wang X, Huang Y, Yan M, Li J, Ding C, Jin H, Fang F, Yang Y, Wu B, Chen D. Wang X, et al. Sci Rep. 2017 Oct 20;7(1):13686. doi: 10.1038/s41598-017-14034-3. Sci Rep. 2017. PMID: 29057985 Free PMC article.

6

Mandibuloacral dysplasia type A-associated progeria caused by homozygous LMNA mutation in a family from Southern China.

Luo DQ, Wang XZ, Meng Y, He DY, Chen YM, Ke ZY, Yan M, Huang Y, Chen DF. Luo DQ, et al. Among authors: wang xz. BMC Pediatr. 2014 Oct 7;14:256. doi: 10.1186/1471-2431-14-256. BMC Pediatr. 2014. PMID: 25286833 Free PMC article.

7

[Genotype, phenotype analysis and follow-up study on patients with Duchenne/Becker muscular dystrophy].

Zhang YZ, Xiong H, Wang XZ, Wang S, Luo J, Wang JM, Jiang YW, Chang XZ, Pan H, Qi JG, Li WZ, Yuan Y, Wu XR. Zhang YZ, et al. Among authors: wang xz, wang jm, wang s. Beijing Da Xue Xue Bao Yi Xue Ban. 2010 Dec 18;42(6):661-6. Beijing Da Xue Xue Bao Yi Xue Ban. 2010. PMID: 21170096 Free article. Chinese.

8

[Detection of subtelomeric rearrangements in patients with idiopathic mental retardation/developmental delay].

Wu Y, Jiang YW, Wang XZ, Wang HF, Wang JM, Yang YL, Qin J, Zhong N, Wu XR. Wu Y, et al. Among authors: wang hf, wang xz, wang jm. Zhonghua Er Ke Za Zhi. 2007 Dec;45(12):906-11. Zhonghua Er Ke Za Zhi. 2007. PMID: 18339278 Chinese.

9

[Methylation-specific multiplex ligation-dependent probe amplification in diagnosis of Prader-Willi syndrome and Angelman syndrome].

Li MR, Wang XZ, Liu XY, Yang YL, Bao XH, Zhang YH, Xiong H, Zhong N, Qin J, Wu XR, Pan H. Li MR, et al. Among authors: wang xz. Zhonghua Yi Xue Za Zhi. 2008 Dec 16;88(46):3257-61. Zhonghua Yi Xue Za Zhi. 2008. PMID: 19159549 Chinese.

10

Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation.

Wu Y, Ji T, Wang J, Xiao J, Wang H, Li J, Gao Z, Yang Y, Cai B, Wang L, Zhou Z, Tian L, Wang X, Zhong N, Qin J, Wu X, Jiang Y. Wu Y, et al. BMC Med Genet. 2010 May 11;11:72. doi: 10.1186/1471-2350-11-72. BMC Med Genet. 2010. PMID: 20459802 Free PMC article.

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