Mo X - Search Results

1

Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery.

Hu Y, Zhu X, Yang Y, Mo X, Sheng M, Yao J, Wang D. Hu Y, et al. Among authors: mo x. Cardiol Young. 2009 Apr;19(2):179-84. doi: 10.1017/S1047951109003667. Epub 2009 Feb 19. Cardiol Young. 2009. PMID: 19224675

2

[Mutation analysis of the CHD7 gene in patients with congenital heart disease].

Qi Q, Yi L, Yang C, Chen H, Shen L, Mo X, Hu Y, Wang Y. Qi Q, et al. Among authors: mo x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Dec;25(6):637-41. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 19065520 Chinese.

3

A novel competitive fluorescent multiplex STR polymorphism assay for rapid, reliable and single-tube screening of 22q11.2 copy-number aberrations.

Yang C, Shen L, Xu Z, Wu X, Mo X, Zhang J, Wang D, Wang Y, Peng Y, Cao L, Jiang Y, Gu H, Chen S, Bian X, Liu J, Qiao D, Yi L. Yang C, et al. Among authors: mo x. Electrophoresis. 2009 Feb;30(3):465-71. doi: 10.1002/elps.200800321. Electrophoresis. 2009. PMID: 19145597

4

Influence of chromosome 22q11.2 microdeletion on postoperative calcium level after cardiac-correction surgery.

Shen L, Gu H, Wang D, Yang C, Xu Z, Jing H, Jiang Y, Ding Y, Hou H, Ge Z, Chen S, Mo X, Yi L. Shen L, et al. Among authors: mo x. Pediatr Cardiol. 2011 Oct;32(7):904-9. doi: 10.1007/s00246-011-0012-y. Epub 2011 Jun 16. Pediatr Cardiol. 2011. PMID: 21678063

5

Common variations in BMP4 confer genetic susceptibility to sporadic congenital heart disease in a Han Chinese population.

Qian B, Mo R, Da M, Peng W, Hu Y, Mo X. Qian B, et al. Among authors: mo r, mo x. Pediatr Cardiol. 2014 Dec;35(8):1442-7. doi: 10.1007/s00246-014-0951-1. Epub 2014 Jul 15. Pediatr Cardiol. 2014. PMID: 25022354 Free PMC article.

6

ECE1 polymorphisms may contribute to the susceptibility of sporadic congenital heart disease in a Chinese population.

Wang Y, Liu Y, Peng W, Wang M, Sun J, Zhang Z, Mo X. Wang Y, et al. Among authors: mo x. DNA Cell Biol. 2012 Aug;31(8):1425-30. doi: 10.1089/dna.2012.1626. Epub 2012 Jun 25. DNA Cell Biol. 2012. PMID: 22731820

7

Association between methionine synthase reductase A66G polymorphism and the risk of congenital heart defects: evidence from eight case-control studies.

Yu D, Yang L, Shen S, Fan C, Zhang W, Mo X. Yu D, et al. Among authors: mo x. Pediatr Cardiol. 2014 Oct;35(7):1091-8. doi: 10.1007/s00246-014-0948-9. Epub 2014 Jun 10. Pediatr Cardiol. 2014. PMID: 24913415 Review.

8

Novel missense variants of ZFPM2/FOG2 identified in conotruncal heart defect patients do not impair interaction with GATA4.

Zhang W, Shen L, Deng Z, Ding Y, Mo X, Xu Z, Gao Q, Yi L. Zhang W, et al. Among authors: mo x. PLoS One. 2014 Jul 15;9(7):e102379. doi: 10.1371/journal.pone.0102379. eCollection 2014. PLoS One. 2014. PMID: 25025186 Free PMC article.

9

Maternal parity and the risk of congenital heart defects in offspring: a dose-response meta-analysis of epidemiological observational studies.

Feng Y, Yu D, Chen T, Liu J, Tong X, Yang L, Da M, Shen S, Fan C, Wang S, Mo X. Feng Y, et al. Among authors: mo x. PLoS One. 2014 Oct 8;9(10):e108944. doi: 10.1371/journal.pone.0108944. eCollection 2014. PLoS One. 2014. PMID: 25295723 Free PMC article.

10

Maternal reproductive history and the risk of congenital heart defects in offspring: a systematic review and meta-analysis.

Feng Y, Wang S, Zhao L, Yu D, Hu L, Mo X. Feng Y, et al. Among authors: mo x. Pediatr Cardiol. 2015 Feb;36(2):253-63. doi: 10.1007/s00246-014-1079-z. Epub 2014 Dec 12. Pediatr Cardiol. 2015. PMID: 25500695 Review.

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