Wang J - Search Results

1

Homeobox C9 is not potentially related to congenital heart disease in Chinese patients.

Sun L, Cheng L, Li C, Gao B, Wang B, Wang J, Wang X, Huang T, Li H, Ma X. Sun L, et al. Among authors: wang x, wang j, wang b. Genet Test Mol Biomarkers. 2012 May;16(5):439-41. doi: 10.1089/gtmb.2011.0217. Epub 2011 Nov 22. Genet Test Mol Biomarkers. 2012. PMID: 22106857 Free PMC article.

2

Novel mutations of NODAL gene in Chinese patients with congenital heart disease.

Sun L, Cheng L, Dong H, Wang B, Huang G, Li Z, Xie X, Shen A, Li X, Wang J, Li H, Ma X. Sun L, et al. Among authors: wang j, wang b. Genet Test Mol Biomarkers. 2012 Apr;16(4):306-9. doi: 10.1089/gtmb.2011.0101. Epub 2012 Feb 21. Genet Test Mol Biomarkers. 2012. PMID: 22352765

3

The HHEX gene is not related to congenital heart disease in 296 Chinese patients.

Deng XP, Zhao LX, Wang BB, Wang J, Cheng LF, Cheng Z, Suo PS, Li H, Ma X. Deng XP, et al. Among authors: wang bb, wang j. World J Pediatr. 2013 Aug;9(3):278-80. doi: 10.1007/s12519-013-0430-4. Epub 2013 Aug 9. World J Pediatr. 2013. PMID: 23929257

4

Identifying novel mutations of NKX2-5 congenital heart disease patients of Chinese minority groups.

Wang J, Chen Q, Wang L, Zhou S, Cheng L, Xie X, Huang G, Wang B, Ma X. Wang J, et al. Among authors: wang l, wang b. Int J Cardiol. 2011 Apr 1;148(1):102-4. doi: 10.1016/j.ijcard.2010.05.041. Epub 2011 Jan 22. Int J Cardiol. 2011. PMID: 21262546 No abstract available.

5

Two novel mutations of the IRX4 gene in patients with congenital heart disease.

Cheng Z, Wang J, Su D, Pan H, Huang G, Li X, Li Z, Shen A, Xie X, Wang B, Ma X. Cheng Z, et al. Among authors: wang j, wang b. Hum Genet. 2011 Nov;130(5):657-62. doi: 10.1007/s00439-011-0996-7. Epub 2011 May 5. Hum Genet. 2011. PMID: 21544582

6

HOXA1 gene is not potentially related to ventricular septal defect in Chinese children.

Liu J, Wang B, Chen X, Li H, Wang J, Cheng L, Ma X, Gao B. Liu J, et al. Among authors: wang j, wang b. Pediatr Cardiol. 2013 Feb;34(2):226-30. doi: 10.1007/s00246-012-0418-1. Epub 2012 Jul 10. Pediatr Cardiol. 2013. PMID: 22777240

7

Variations of the COL1A1 gene promoter and the relation to developmental dysplasia of the hip.

Zhao L, Tian W, Pan H, Zhu X, Wang J, Cheng Z, Cheng L, Ma X, Wang B. Zhao L, et al. Among authors: wang j, wang b. Genet Test Mol Biomarkers. 2013 Nov;17(11):840-3. doi: 10.1089/gtmb.2013.0179. Epub 2013 Aug 13. Genet Test Mol Biomarkers. 2013. PMID: 23941072

8

A novel mutation of Hyaluronan synthase 2 gene in Chinese children with ventricular septal defect.

Zhu X, Deng X, Huang G, Wang J, Yang J, Chen S, Ma X, Wang B. Zhu X, et al. Among authors: wang j, wang b. PLoS One. 2014 Feb 18;9(2):e87437. doi: 10.1371/journal.pone.0087437. eCollection 2014. PLoS One. 2014. PMID: 24558368 Free PMC article.

9

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family.

Wang B, Xu B, Cheng Z, Zhou X, Wang J, Yang G, Cheng L, Yang J, Ma X. Wang B, et al. Among authors: wang j. Clin Chim Acta. 2012 Jul 11;413(13-14):1049-52. doi: 10.1016/j.cca.2012.02.015. Epub 2012 Feb 22. Clin Chim Acta. 2012. PMID: 22374128

10

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens.

Li H, Wen Q, Li H, Zhao L, Zhang X, Wang J, Cheng L, Yang J, Chen S, Ma X, Wang B. Li H, et al. Among authors: wang j, wang b. J Cyst Fibros. 2012 Jul;11(4):316-23. doi: 10.1016/j.jcf.2012.01.005. Epub 2012 Apr 6. J Cyst Fibros. 2012. PMID: 22483971 Free article.

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