Yi L - Search Results

1

[Prenatal genetic study of fetuses with congenital heart diseases].

Xu ZF, Cao L, Ji XQ, Yang C, Zhang JJ, Xu QJ, Zha W, Yang YQ, Lin YS, Chen CH, Liu A, Li L, Lin Y, Yi L. Xu ZF, et al. Among authors: yi l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Apr;26(2):128-33. doi: 10.3760/cma.j.issn.1003-9406.2009.02.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19350500 Chinese.

2

22q11.2 microduplication in a family with recurrent fetal congenital heart disease.

Hu P, Ji X, Yang C, Zhang J, Lin Y, Cheng J, Ma D, Cao L, Yi L, Xu Z. Hu P, et al. Among authors: yi l. Eur J Med Genet. 2011 Jul-Aug;54(4):e433-6. doi: 10.1016/j.ejmg.2011.03.009. Epub 2011 Apr 5. Eur J Med Genet. 2011. PMID: 21473936

3

[Application of multiplex ligation-dependent probe amplification for rapid detection of aneuploidies in prenatal diagnosis].

Ma DY, Hu P, Zhang JJ, Yi L, Ji XQ, Yang C, Cheng J, Li L, Lin Y, Xu ZF. Ma DY, et al. Among authors: yi l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Oct;28(5):543-7. doi: 10.3760/cma.j.issn.1003-9406.2011.05.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21983731 Chinese.

4

[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: yi l. 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.

5

[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: yi l. 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.

6

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: yi l. Electrophoresis. 2009 Feb;30(3):465-71. doi: 10.1002/elps.200800321. Electrophoresis. 2009. PMID: 19145597

7

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: yi l. Pediatr Cardiol. 2011 Oct;32(7):904-9. doi: 10.1007/s00246-011-0012-y. Epub 2011 Jun 16. Pediatr Cardiol. 2011. PMID: 21678063

8

Functional variant in microRNA-196a2 contributes to the susceptibility of congenital heart disease in a Chinese population.

Xu J, Hu Z, Xu Z, Gu H, Yi L, Cao H, Chen J, Tian T, Liang J, Lin Y, Qiu W, Ma H, Shen H, Chen Y. Xu J, et al. Among authors: yi l. Hum Mutat. 2009 Aug;30(8):1231-6. doi: 10.1002/humu.21044. Hum Mutat. 2009. PMID: 19514064 Free article.

9

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. 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

10

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: yi l. 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

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