Wu XR - Search Results

1

[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: wu xr. Zhonghua Er Ke Za Zhi. 2007 Dec;45(12):906-11. Zhonghua Er Ke Za Zhi. 2007. PMID: 18339278 Chinese.

2

[Clinical characteristics of alternating hemiplegia of childhood in 13 patients].

Zhang YH, Sun WX, Qin J, Jiang YW, Wu XR. Zhang YH, et al. Among authors: wu xr. Zhonghua Er Ke Za Zhi. 2003 Sep;41(9):680-3. Zhonghua Er Ke Za Zhi. 2003. PMID: 14733811 Chinese.

3

[Screening for carrier and prenatal diagnosis of X-linked adrenoleukodystrophy].

Wang AH, Bao XH, Xiong H, Pan H, Wu Y, Zhang YH, Shi CY, Qin J, Wu XR. Wang AH, et al. Among authors: wu y, wu xr. Zhonghua Er Ke Za Zhi. 2005 May;43(5):345-9. Zhonghua Er Ke Za Zhi. 2005. PMID: 15924749 Chinese.

4

[Clinical characteristics of cases with leukoencephalopathy with vanishing white matter].

Wu Y, Jiang YW, Qin J, Xiao JX, Wang JM, Yang YL, Zhang YH, Chang XZ, Lin Q, Wu XR. Wu Y, et al. Among authors: wu xr. Zhonghua Er Ke Za Zhi. 2007 Feb;45(2):115-20. Zhonghua Er Ke Za Zhi. 2007. PMID: 17456339 Chinese.

5

[Clinical features and genotype-phenotype studies of 89 Chinese patients with X-linked adrenoleukodystrophy].

Ping LL, Bao XH, Wang AH, Pan H, Wu Y, Xiong H, Jiang YW, Qin J, Wu XR. Ping LL, et al. Among authors: wu y, wu xr. Zhonghua Er Ke Za Zhi. 2007 Mar;45(3):203-7. Zhonghua Er Ke Za Zhi. 2007. PMID: 17504626 Chinese.

6

[Clinical studies on fifty-seven Chinese patients with combined methylmalonic aciduria and homocysteinemia].

Zhang Y, Song JQ, Liu P, Yan R, Dong JH, Yang YL, Wang LF, Jiang YW, Zhang YH, Qin J, Wu XR. Zhang Y, et al. Among authors: wu xr. Zhonghua Er Ke Za Zhi. 2007 Jul;45(7):513-7. Zhonghua Er Ke Za Zhi. 2007. PMID: 17953808 Clinical Trial. Chinese.

7

[Clinical and genetic analysis of a family with Pelizaeus-Merzbacher disease].

Wang HF, Wu Y, Jiang YW, Wang JM, Tang MK, Zhang YH, Qin J, Lin Q, Wu XR. Wang HF, et al. Among authors: wu y, wu xr. Zhonghua Er Ke Za Zhi. 2007 Dec;45(12):912-6. Zhonghua Er Ke Za Zhi. 2007. PMID: 18339279 Chinese.

8

Proteolipid protein 1 gene mutation in nine patients with Pelizaeus-Merzbacher disease.

Wang JM, Wu Y, Wang HF, Deng YH, Yang YL, Qin J, Li XY, Wu XR, Jiang YW. Wang JM, et al. Among authors: wu y, wu xr. Chin Med J (Engl). 2008 Sep 5;121(17):1638-42. Chin Med J (Engl). 2008. PMID: 19024090

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: wu xr. Zhonghua Yi Xue Za Zhi. 2008 Dec 16;88(46):3257-61. Zhonghua Yi Xue Za Zhi. 2008. PMID: 19159549 Chinese.

10

[Multiplex ligation-dependent probe amplification analysis of subtelomeric chromosome rearrangements in children with idiopathic mental retardation].

Li MR, Wang XZ, Yang YL, Zhang YH, Xiong H, Bao XH, Zhong N, Wu XR, Pan H. Li MR, et al. Among authors: wu xr. Zhonghua Yi Xue Za Zhi. 2009 Nov 3;89(40):2839-42. Zhonghua Yi Xue Za Zhi. 2009. PMID: 20137665 Chinese.

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