Su L - Search Results

1

Chromosomal abnormalities and copy number variations in fetal ventricular septal defects.

Cai M, Huang H, Su L, Lin N, Wu X, Xie X, An G, Li Y, Lin Y, Xu L, Cao H. Cai M, et al. Among authors: su l. Mol Cytogenet. 2018 Nov 28;11:58. doi: 10.1186/s13039-018-0408-y. eCollection 2018. Mol Cytogenet. 2018. PMID: 30519285 Free PMC article.

2

[Prenatal diagnosis of 22q11 microdeletion syndrome].

Cai M, Huang H, Lin N, Guo N, Wu X, Su L, Xu L. Cai M, et al. Among authors: su l. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):192-195. doi: 10.3760/cma.j.issn.1003-9406.2017.02.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397216 Chinese.

3

Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome.

Cai M, Huang H, Su L, Lin N, Wu X, Xie X, An G, Li Y, Lin Y, Xu L. Cai M, et al. Among authors: su l. Medicine (Baltimore). 2018 Dec;97(50):e13617. doi: 10.1097/MD.0000000000013617. Medicine (Baltimore). 2018. PMID: 30558042 Free PMC article.

4

Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype.

Su L, Huang H, An G, Cai M, Wu X, Li Y, Xie X, Lin Y, Wang M, Xu L. Su L, et al. Mol Genet Genomic Med. 2019 Aug;7(8):e811. doi: 10.1002/mgg3.811. Epub 2019 Jun 17. Mol Genet Genomic Med. 2019. PMID: 31209990 Free PMC article.

5

Submicroscopic aberrations of chromosome 16 in prenatal diagnosis.

Wu X, Xu L, Li Y, Lin N, Su L, Cai M, Xie X, Zheng L, Huang H, Lin Y. Wu X, et al. Among authors: su l. Mol Cytogenet. 2019 Aug 5;12:36. doi: 10.1186/s13039-019-0448-y. eCollection 2019. Mol Cytogenet. 2019. PMID: 31391865 Free PMC article.

6

Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays.

Cai M, Lin N, Su L, Wu X, Xie X, Li Y, Chen X, Dai Y, Lin Y, Huang H, Xu L. Cai M, et al. Among authors: su l. J Clin Lab Anal. 2020 Jan;34(1):e23025. doi: 10.1002/jcla.23025. Epub 2019 Sep 10. J Clin Lab Anal. 2020. PMID: 31506986 Free PMC article.

7

Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age.

Wu X, An G, Xie X, Su L, Cai M, Chen X, Li Y, Lin N, He D, Wang M, Huang H, Xu L. Wu X, et al. Among authors: su l. J Clin Lab Anal. 2020 Apr;34(4):e23117. doi: 10.1002/jcla.23117. Epub 2019 Nov 24. J Clin Lab Anal. 2020. PMID: 31762079 Free PMC article.

8

Copy number variations associated with fetal congenital kidney malformations.

Cai M, Lin N, Su L, Wu X, Xie X, Li Y, Chen X, Lin Y, Huang H, Xu L. Cai M, et al. Among authors: su l. Mol Cytogenet. 2020 Mar 24;13:11. doi: 10.1186/s13039-020-00481-7. eCollection 2020. Mol Cytogenet. 2020. PMID: 32211073 Free PMC article.

9

Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.

Wu X, Li Y, Su L, Xie X, Cai M, Lin N, Huang H, Lin Y, Xu L. Wu X, et al. Among authors: su l. Mol Diagn Ther. 2020 Oct;24(5):611-619. doi: 10.1007/s40291-020-00474-7. Mol Diagn Ther. 2020. PMID: 32651932 Free PMC article.

10

Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes.

Cai M, Lin N, Su L, Wu X, Xie X, Li Y, Lin Y, Xu L, Huang H. Cai M, et al. Among authors: su l. Sci Rep. 2020 Sep 15;10(1):15094. doi: 10.1038/s41598-020-72157-6. Sci Rep. 2020. PMID: 32934329 Free PMC article.

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