Wang N - Search Results

1

Modification of phenotype by SMN2 copy numbers in two Chinese families with SMN1 deletion in two continuous generations.

Chen WJ, He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N. Chen WJ, et al. Among authors: wang n. Clin Chim Acta. 2012 Nov 20;413(23-24):1855-60. doi: 10.1016/j.cca.2012.07.020. Epub 2012 Aug 4. Clin Chim Acta. 2012. PMID: 22884440

2

Molecular diagnosis and prophylactic therapy for presymptomatic Chinese patients with Wilson disease.

Wu ZY, Lin MT, Murong SX, Wang N. Wu ZY, et al. Among authors: wang n. Arch Neurol. 2003 May;60(5):737-41. doi: 10.1001/archneur.60.5.737. Arch Neurol. 2003. PMID: 12756138 Clinical Trial.

3

[Genotype-phenotype correlation of patients with wilson disease in Chinese population].

Wu ZY, Wang N, Lin MT, Fang L, Murong SX. Wu ZY, et al. Among authors: wang n. Zhonghua Yi Xue Za Zhi. 2003 Feb 25;83(4):309-11. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12812649 Chinese.

4

[Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy].

Wang N, Wu ZY, Wang CD, Wang ZQ, Lin MT, Fang L, Murong SX. Wang N, et al. Among authors: wang cd, wang zq. Zhonghua Yi Xue Za Zhi. 2003 Apr 25;83(8):650-3. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12887821 Chinese.

5

[The quantitative analysis of protein particles of erythrocyte membrane from Duchenne muscular dystrophy patients and the gene carriers].

Hong ZL, Murong SX, Zhong XR, Lin MT, Cheng WL, Lin X, Wang N. Hong ZL, et al. Among authors: wang n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb;21(1):68-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 14767914 Chinese.

6

FSHD in Chinese population: characteristics of translocation and genotype-phenotype correlation.

Wu ZY, Wang ZQ, Murong SX, Wang N. Wu ZY, et al. Among authors: wang n, wang zq. Neurology. 2004 Aug 10;63(3):581-3. doi: 10.1212/01.wnl.0000133210.93075.81. Neurology. 2004. PMID: 15304602

7

[Study on EcoR I fragment polymorphism of the subtelomeric domains within 4q35 and 10q26 with pulsed field gel electrophoresis in the Chinese population].

Wu ZY, Wang ZQ, Wang N, Lin MT, Murong SX. Wu ZY, et al. Among authors: wang n, wang zq. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):552-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583980 Chinese.

8

Gene symbol: GTP cyclohydrolase I (GCH-I). Disease: dopa-responsive dystonia.

Hui xie H, Wu ZY, Wang N, Murong SX. Hui xie H, et al. Among authors: wang n. Hum Genet. 2005 Feb;116(3):235. Hum Genet. 2005. PMID: 15818812 No abstract available.

9

Rapid diagnosis of spinal muscular atrophy using denaturing high-performance liquid chromatography.

Chen WJ, Wu ZY, Wang N, Lin MT, Mu-Rong SX. Chen WJ, et al. Among authors: wang n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):291-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952118

10

[Prevalence of CYP2C19 polymorphisms involved in clopidogrel metabolism in Fujian Han population].

Wei W, Fang L, Wang N, Zhang T, Zeng JB, Lin MT. Wei W, et al. Among authors: wang n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):420-5. doi: 10.3760/cma.j.issn.1003-9406.2012.04.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875498 Chinese.

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