Murong SX - Search Results

1

Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.

He J, Zhang QJ, Lin QF, Chen YF, Lin XZ, Lin MT, Murong SX, Wang N, Chen WJ. He J, et al. Among authors: murong sx. Gene. 2013 Apr 15;518(2):325-9. doi: 10.1016/j.gene.2012.12.109. Epub 2013 Jan 23. Gene. 2013. PMID: 23352792

2

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. 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

3

Quantitative studies on SMN1 gene and carrier testing of spinal muscular atrophy.

Chen WJ, Wu ZY, Wang N, Lin MT, Mu-rong SX. Chen WJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Dec;22(6):559-602. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16331551

4

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

5

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: murong sx. 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

6

Molecular analysis of the dystrophin gene in 407 Chinese patients with Duchenne/Becker muscular dystrophy by the combination of multiplex ligation-dependent probe amplification and Sanger sequencing.

Chen WJ, Lin QF, Zhang QJ, He J, Liu XY, Lin MT, Murong SX, Liou CW, Wang N. Chen WJ, et al. Among authors: murong sx. Clin Chim Acta. 2013 Aug 23;423:35-8. doi: 10.1016/j.cca.2013.04.006. Epub 2013 Apr 13. Clin Chim Acta. 2013. PMID: 23588064

7

Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification.

Chen WJ, Yao XP, Zhang QJ, Ni W, He J, Li HF, Liu XY, Zhao GX, Murong SX, Wang N, Wu ZY. Chen WJ, et al. Among authors: murong sx. Gene. 2013 Oct 15;529(1):159-62. doi: 10.1016/j.gene.2013.07.071. Epub 2013 Aug 11. Gene. 2013. PMID: 23939468

8

Variations of IGHMBP2 gene was not the major cause of Han Chinese patients with non-5q-spinal muscular atrophies.

Lin X, Zhang QJ, He J, Lin MT, Murong SX, Wang N, Chen WJ. Lin X, et al. Among authors: murong sx. J Child Neurol. 2014 Aug;29(8):NP35-9. doi: 10.1177/0883073813497827. Epub 2013 Sep 9. J Child Neurol. 2014. PMID: 24022109

9

New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 Patients.

Lin F, Wang ZQ, Lin MT, Murong SX, Wang N. Lin F, et al. Among authors: murong sx. Chin Med J (Engl). 2015 Jul 5;128(13):1707-13. doi: 10.4103/0366-6999.159336. Chin Med J (Engl). 2015. PMID: 26112708 Free PMC article.

10

Rapid diagnosis of spinal muscular atrophy using high-resolution melting analysis.

Chen WJ, Dong WJ, Lin XZ, Lin MT, Murong SX, Wu ZY, Wang N. Chen WJ, et al. Among authors: murong sx. BMC Med Genet. 2009 May 29;10:45. doi: 10.1186/1471-2350-10-45. BMC Med Genet. 2009. PMID: 19480685 Free PMC article.

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