Murong SX - Search Results

1

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: murong sx. Neurology. 2004 Aug 10;63(3):581-3. doi: 10.1212/01.wnl.0000133210.93075.81. Neurology. 2004. PMID: 15304602

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: murong sx. 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: murong sx. 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: murong sx. Zhonghua Yi Xue Za Zhi. 2003 Apr 25;83(8):650-3. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12887821 Chinese.

5

[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: murong sx. 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.

6

Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis.

Chen WJ, Wu ZY, Lin MT, Su JF, Lin Y, Murong SX, Wang N. Chen WJ, et al. Among authors: murong sx. Arch Neurol. 2007 Feb;64(2):225-31. doi: 10.1001/archneur.64.2.225. Arch Neurol. 2007. PMID: 17296838

7

[Analysis of alleles 4qA and 4qB of the chromosome 4q subtelomere in Chinese Han population].

Chen ZJ, Wang ZQ, Wu ZY, Wang N, Lin MT, Murong SX. Chen ZJ, et al. Among authors: murong sx. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Jun;24(3):334-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17557251 Chinese.

8

A novel mutation in the senataxin gene identified in a Chinese patient with sporadic amyotrophic lateral sclerosis.

Zhao ZH, Chen WZ, Wu ZY, Wang N, Zhao GX, Chen WJ, Murong SX. Zhao ZH, et al. Among authors: murong sx. Amyotroph Lateral Scler. 2009 Apr;10(2):118-22. doi: 10.1080/17482960802572673. Amyotroph Lateral Scler. 2009. PMID: 19058054

9

[Characteristics of gene structure in facioscapulohumeral muscular dystrophy-related 4q35 subtelomere and genotype-phenotype correlation in Chinese Han population].

Wang ZQ, Wu ZY, Wang N, Lin MT, Murong SX. Wang ZQ, et al. Among authors: murong sx. Zhonghua Yi Xue Za Zhi. 2009 Feb 10;89(5):304-9. Zhonghua Yi Xue Za Zhi. 2009. PMID: 19563705 Chinese.

10

Distinguishing the 4qA and 4qB variants is essential for the diagnosis of facioscapulohumeral muscular dystrophy in the Chinese population.

Wang ZQ, Wang N, van der Maarel S, Murong SX, Wu ZY. Wang ZQ, et al. Among authors: murong sx. Eur J Hum Genet. 2011 Jan;19(1):64-9. doi: 10.1038/ejhg.2010.143. Epub 2010 Aug 25. Eur J Hum Genet. 2011. PMID: 20736973 Free PMC article.

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