Wang J - Search Results

1

Wang B, Zhou S, Chen Q, Xie X, Huang G, Wang J, Zhoua S, Ma X. Wang B, et al. Among authors: wang j. Int J Cardiol. 2011 Feb 3;146(3):415-6. doi: 10.1016/j.ijcard.2009.12.013. Epub 2010 Feb 24. Int J Cardiol. 2011. PMID: 20181399

2

Genetic variation of SAL-Like 4 (SALL4) in ventricular septal defect.

Wang B, Li L, Xie X, Wang J, Yan J, Mu Y, Ma X. Wang B, et al. Among authors: wang j. Int J Cardiol. 2010 Nov 19;145(2):224-226. doi: 10.1016/j.ijcard.2009.05.067. Epub 2009 Jul 19. Int J Cardiol. 2010. PMID: 19619907

3

CFC1 mutations in Chinese children with congenital heart disease.

Wang B, Wang J, Liu S, Han X, Xie X, Tao Y, Yan J, Ma X. Wang B, et al. Among authors: wang j. Int J Cardiol. 2011 Jan 7;146(1):86-8. doi: 10.1016/j.ijcard.2009.07.034. Epub 2009 Oct 23. Int J Cardiol. 2011. PMID: 19853937

4

Teratocarcinoma-derived growth factor 1 (TDGF1) sequence variants in patients with congenital heart defect.

Wang B, Yan J, Peng Z, Wang J, Liu S, Xie X, Ma X. Wang B, et al. Among authors: wang j. Int J Cardiol. 2011 Jan 21;146(2):225-7. doi: 10.1016/j.ijcard.2009.08.046. Epub 2009 Oct 24. Int J Cardiol. 2011. PMID: 19853938

5

Spatial pattern and variations in the prevalence of congenital heart disease in children aged 4-18 years in the Qinghai-Tibetan Plateau.

Ma LG, Chen QH, Wang YY, Wang J, Ren ZP, Cao ZF, Cao YR, Ma X, Wang BB. Ma LG, et al. Among authors: wang yy, wang bb, wang j. Sci Total Environ. 2018 Jun 15;627:158-165. doi: 10.1016/j.scitotenv.2018.01.194. Epub 2018 Feb 3. Sci Total Environ. 2018. PMID: 29426137

6

Identification of LBX2 as a novel causal gene of atrial septal defect.

Wang J, Luo J, Chen Q, Wang X, He J, Zhang W, Yin Z, Zheng F, Pan H, Li T, Lou Q, Wang B. Wang J, et al. Among authors: wang x, wang b. Int J Cardiol. 2018 Aug 15;265:188-194. doi: 10.1016/j.ijcard.2018.04.038. Epub 2018 Apr 11. Int J Cardiol. 2018. PMID: 29669692

7

Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect.

Wang B, Yan J, Mi R, Zhou S, Xie X, Wang J, Ma X. Wang B, et al. Among authors: wang j. Int J Cardiol. 2010 Nov 5;145(1):83-5. doi: 10.1016/j.ijcard.2009.05.030. Epub 2009 Jun 13. Int J Cardiol. 2010. PMID: 19525021

8

Mutation analysis of Connexon43 gene in Chinese patients with congenital heart defects.

Wang B, Wen Q, Xie X, Liu S, Liu M, Tao Y, Li Z, Suo P, Shen A, Wang J, Ma X. Wang B, et al. Among authors: wang j. Int J Cardiol. 2010 Dec 3;145(3):487-9. doi: 10.1016/j.ijcard.2009.06.026. Epub 2009 Jul 16. Int J Cardiol. 2010. PMID: 19615768 No abstract available.

9

GPR3 may not be a potential candidate gene for premature ovarian failure.

Zhou S, Wang B, Ni F, Wang J, Cao Y, Ma X. Zhou S, et al. Among authors: wang j, wang b. Reprod Biomed Online. 2010 Jan;20(1):53-5. doi: 10.1016/j.rbmo.2009.10.013. Epub 2009 Oct 30. Reprod Biomed Online. 2010. PMID: 20158988

10

Polyalanine repeat expansion mutation of the HOXD13 gene in a Chinese family with unusual clinical manifestations of synpolydactyly.

Gong L, Wang B, Wang J, Yu H, Ma X, Yang J. Gong L, et al. Among authors: wang j, wang b. Eur J Med Genet. 2011 Mar-Apr;54(2):108-11. doi: 10.1016/j.ejmg.2010.10.007. Epub 2010 Oct 23. Eur J Med Genet. 2011. PMID: 20974300

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