Cao L - Search Results

1

Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study.

Wang Y, Cao L, Liang D, Meng L, Wu Y, Qiao F, Ji X, Luo C, Zhang J, Xu T, Yu B, Wang L, Wang T, Pan Q, Ma D, Hu P, Xu Z. Wang Y, et al. Among authors: cao l. Am J Obstet Gynecol. 2018 Feb;218(2):244.e1-244.e17. doi: 10.1016/j.ajog.2017.10.225. Epub 2017 Nov 8. Am J Obstet Gynecol. 2018. PMID: 29128521 Clinical Trial.

2

[Detection of cryptic copy number variations in a fetus with congenital heart disease by array-based comparative genomic hybridization].

HU P, WANG Y, JI XQ, LIN Y, Li L, ZHOU XY, CHEN J, MA DY, CAO L, Xu Z. HU P, et al. Among authors: cao l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Apr;28(2):133-6. doi: 10.3760/cma.j.issn.1003-9406.2011.02.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21462121 Chinese.

3

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: cao 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

4

[Prenatal diagnosis of 22q11.2 microdeletion by multiplex ligation-dependent probe amplification].

Luo CY, Ma DY, Zhang JJ, Hu P, Cao L, Ji XQ, Zhou J, Liu A, Wu Y, Cheng J, Lin Y, Xu ZF. Luo CY, et al. Among authors: cao l. Zhonghua Fu Chan Ke Za Zhi. 2013 Nov;48(11):824-7. Zhonghua Fu Chan Ke Za Zhi. 2013. PMID: 24444558 Chinese.

5

[Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome].

Ji X, Hu H, Wang Y, Liang D, Luo C, Meng L, Zhou J, Cao L, Ma D, Hu P, Xu Z. Ji X, et al. Among authors: cao l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):853-856. doi: 10.3760/cma.j.issn.1003-9406.2017.06.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188615 Chinese.

6

[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: cao 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.

7

[Cytogenetic analysis of a complex chromosomal imbalance 14q+ in a fetus featuring multiple congenital defects].

Li L, Zhou XY, Ji XQ, Yang YQ, Cao L, Zhou J, Liu A, Cheng J, Liu Y, Hu P, Xu ZF. Li L, et al. Among authors: cao l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Apr;29(2):214-7. doi: 10.3760/cma.j.issn.1003-9406.2012.02.021. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22487837 Chinese.

8

[Array-based comparative genomic hybridization detection of copy number variations in a fetus with hypoplastic left-heart syndrome].

Wang Y, Ma DY, Yang YQ, Zhou J, Zhou XY, Ji XQ, Chen J, Cao L, Hu P, Xu ZF. Wang Y, et al. Among authors: cao l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Aug;29(4):439-42. doi: 10.3760/cma.j.issn.1003-9406.2012.04.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22875502 Chinese.

9

Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect.

Zhang J, Ma D, Wang Y, Cao L, Wu Y, Qiao F, Liu A, Li L, Lin Y, Liu G, Liu C, Hu P, Xu Z. Zhang J, et al. Among authors: cao l. Mol Cytogenet. 2015 Dec 29;8:100. doi: 10.1186/s13039-015-0209-5. eCollection 2015. Mol Cytogenet. 2015. PMID: 26715944 Free PMC article.

10

Peptidomic Analysis of Fetal Heart Tissue for Identification of Endogenous Peptides Involved in Tetralogy of Fallot.

Zhang J, Liang D, Cheng Q, Cao L, Wu Y, Wang Y, Han S, Yu Z, Cui X, Xu T, Ma D, Hu P, Xu Z. Zhang J, et al. Among authors: cao l. DNA Cell Biol. 2017 Jun;36(6):451-461. doi: 10.1089/dna.2017.3647. Epub 2017 Mar 17. DNA Cell Biol. 2017. PMID: 28304193

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