Shang X - Search Results

1

A splicing mutation in VPS4B causes dentin dysplasia I.

Yang Q, Chen D, Xiong F, Chen D, Liu C, Liu Y, Yu Q, Xiong J, Liu J, Li K, Zhao L, Ye Y, Zhou H, Hu L, Tian Z, Shang X, Zhang L, Wei X, Zhou W, Li D, Zhang W, Xu X. Yang Q, et al. Among authors: shang x. J Med Genet. 2016 Sep;53(9):624-33. doi: 10.1136/jmedgenet-2015-103619. Epub 2016 May 31. J Med Genet. 2016. PMID: 27247351

2

The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity.

Chen W, Zhang X, Shang X, Cai R, Li L, Zhou T, Sun M, Xiong F, Xu X. Chen W, et al. Among authors: shang x. BMC Med Genet. 2010 Feb 25;11:31. doi: 10.1186/1471-2350-11-31. BMC Med Genet. 2010. PMID: 20181291 Free PMC article.

3

Analysis of alpha-hemoglobin-stabilizing protein (AHSP) gene as a genetic modifier to the phenotype of beta-thalassemia in Southern China.

Wang Z, Yu W, Li Y, Shang X, Zhang X, Xiong F, Xu X. Wang Z, et al. Among authors: shang x. Blood Cells Mol Dis. 2010 Aug 15;45(2):128-32. doi: 10.1016/j.bcmd.2010.04.005. Blood Cells Mol Dis. 2010. PMID: 20627634

4

Molecular characterization of a novel 27.6-kb deletion causing α(+) thalassemia in a Chinese family.

Wei XF, Shang X, He DQ, Huang JW, Zhang XH, Xu XM. Wei XF, et al. Among authors: shang x. Ann Hematol. 2011 Jan;90(1):17-22. doi: 10.1007/s00277-010-1030-1. Epub 2010 Jul 20. Ann Hematol. 2011. PMID: 20645100

5

[Prenatal diagnosis of a fetus in a family with mandibulofacial dysostosis].

Liu YH, Shi SQ, Zhang YL, Dai Y, Shang X, Wu YM, Li CQ, Li LF. Liu YH, et al. Among authors: shang x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Aug;27(4):437-40. doi: 10.3760/cma.j.issn.1003-9406.2010.04.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20677153 Chinese.

6

Mutation analysis of 73 southern Chinese Wilson's disease patients: identification of 10 novel mutations and its clinical correlation.

Wang LH, Huang YQ, Shang X, Su QX, Xiong F, Yu QY, Lin HP, Wei ZS, Hong MF, Xu XM. Wang LH, et al. Among authors: shang x. J Hum Genet. 2011 Sep;56(9):660-5. doi: 10.1038/jhg.2011.76. Epub 2011 Jul 28. J Hum Genet. 2011. PMID: 21796144

7

[Large-scale population-based genetic screening and prenatal diagnosis for thalassemias in Zhuhai City of Guangdong Province].

Zhou YQ, Shang X, Yin BM, Xiong F, Xiao QZ, Zhou WJ, Zhang YL, Xu XM. Zhou YQ, et al. Among authors: shang x. Zhonghua Fu Chan Ke Za Zhi. 2012 Feb;47(2):90-5. Zhonghua Fu Chan Ke Za Zhi. 2012. PMID: 22455738 Chinese.

8

Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease.

Xiong F, Li Q, Zhang C, Chen Y, Li P, Wei X, Li Q, Zhou W, Li L, Shang X, Xu X. Xiong F, et al. Among authors: shang x. Cardiovasc Pathol. 2013 Mar-Apr;22(2):141-5. doi: 10.1016/j.carpath.2012.07.001. Epub 2012 Sep 6. Cardiovasc Pathol. 2013. PMID: 22959235

9

Rapid simultaneous genotyping of polymorphisms in ADH1B and ALDH2 using high resolution melting assay.

Yuan XW, Zhou WJ, Shang X, Li L, Liu YH, Xu XM. Yuan XW, et al. Among authors: shang x. Clin Chem Lab Med. 2013 May;51(5):e75-7. doi: 10.1515/cclm-2012-0509. Clin Chem Lab Med. 2013. PMID: 23001317 No abstract available.

10

[Analysis of hematological characteristics on the 79 co-inheritance of α-thalassemia and β-thalassemia carriers in Guangxi].

Xiong F, Lou JW, Wei XF, Sun MN, Huang JW, Shang X, Zhang XH, Xu XM. Xiong F, et al. Among authors: shang x. Zhonghua Xue Ye Xue Za Zhi. 2012 Oct;33(10):856-60. Zhonghua Xue Ye Xue Za Zhi. 2012. PMID: 23384911 Chinese.

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