Mo XM - Search Results

1

[Detection and related analysis to chromosome 22q11 microdeletion in patients with congenital heart diseases].

Xu ZF, Yi L, Mo XM, Hu Y, Wang DJ, Zhu RF, Jiang YZ, Wu X, Wu Z, Shen L, Zhang Y, Zhong XL. Xu ZF, et al. Among authors: mo xm. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Jun;23(3):250-5. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16767657 Chinese.

2

[Surgical treatment of newborns with congenital heart diseases].

Zhang RF, Qian LB, Wang DW, Gu XL, Wang ZX, Mo XM, Gu HT, Xia JH, Wu XS, Zhou XY. Zhang RF, et al. Among authors: mo xm. Zhonghua Yi Xue Za Zhi. 2003 Jan 10;83(1):27-30. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12757641 Chinese.

3

New tetranucleotide STRP markers for detecting the 22q11.2 deletion.

Yi L, Xu ZF, Mo XM, Hu YL, Wang DJ, Han B, Wang Y, Yang C, Jiang YZ, Shen L, Wu X, Zhu RF, Zhou XJ. Yi L, et al. Among authors: mo xm. Mol Cell Probes. 2006 Dec;20(6):359-65. doi: 10.1016/j.mcp.2006.03.008. Epub 2006 May 20. Mol Cell Probes. 2006. PMID: 16774813

4

VEGF C-634G polymorphism is associated with protection from isolated ventricular septal defect: case-control and TDT studies.

Xie J, Yi L, Xu ZF, Mo XM, Hu YL, Wang DJ, Ren HZ, Han B, Wang Y, Yang C, Zhao YL, Shi DQ, Jiang YZ, Shen L, Qiao D, Chen SL, Yu BJ. Xie J, et al. Among authors: mo xm. Eur J Hum Genet. 2007 Dec;15(12):1246-51. doi: 10.1038/sj.ejhg.5201890. Epub 2007 Jul 11. Eur J Hum Genet. 2007. PMID: 17625508

5

[Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation dependent probe amplification].

Yang YH, Hu YL, Zhu XY, Mo XM, Wang DJ, Yao JC, Sheng M, Zhu HY, Li J, Ru T, Wang ZQ. Yang YH, et al. Among authors: mo xm. Zhongguo Dang Dai Er Ke Za Zhi. 2009 Nov;11(11):892-6. Zhongguo Dang Dai Er Ke Za Zhi. 2009. PMID: 20113655 Free article. Chinese.

6

[The individualized surgical treatment of transposition of the great arteries].

Mo XM, Gu HT, Zuo WS, Sun J, Peng W, Qi JR, Shen L, Ding JY, Xia JH, Wang ZX, Qian LB. Mo XM, et al. Zhonghua Wai Ke Za Zhi. 2010 May 15;48(10):734-7. Zhonghua Wai Ke Za Zhi. 2010. PMID: 20646487 Chinese.

7

[Clinical application and experimental studies of the pulsed inhaled nitric oxide flow controlling instrument].

Mo XM, Zhao EC, Wang MS, Gu X, Wang Z, Wang C. Mo XM, et al. Zhongguo Yi Liao Qi Xie Za Zhi. 2002 Jan;26(1):33-5. Zhongguo Yi Liao Qi Xie Za Zhi. 2002. PMID: 16104155 Chinese.

8

[Progress on genetic research on familial congenital heart disease].

Zhang WY, Zhou K, Mo XM. Zhang WY, et al. Among authors: mo xm. Zhonghua Xin Xue Guan Bing Za Zhi. 2013 Sep;41(9):812-4. Zhonghua Xin Xue Guan Bing Za Zhi. 2013. PMID: 24331816 Review. Chinese. No abstract available.

9

Genetic variants of the endothelial NO synthase gene (eNOS) may confer increased risk of sporadic congenital heart disease.

Zhou K, Wang Y, Peng W, Sun J, Qing YM, Mo XM. Zhou K, et al. Among authors: mo xm. Genet Mol Res. 2014 May 16;13(2):3805-11. doi: 10.4238/2014.May.16.4. Genet Mol Res. 2014. PMID: 24938467 Free article.

10

[Application of metabolomics in clinical research on pediatric congenital heart disease].

Du XY, Zhang DY, Zeng XY, Xu XY, Jiang L, Mo XM. Du XY, et al. Among authors: mo xm. Zhonghua Er Ke Za Zhi. 2024 Aug 2;62(8):796-799. doi: 10.3760/cma.j.cn112140-20240429-00300. Zhonghua Er Ke Za Zhi. 2024. PMID: 39039887 Review. Chinese.

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