Liu Y - Search Results

1

Whole exome sequencing aids the diagnosis of Simpson-Golabi-Behmel syndrome in two male fetuses.

Xiang J, Zhang Q, Song X, Liu Y, Li H, Li H, Wang T. Xiang J, et al. Among authors: liu y. J Int Med Res. 2020 Jan;48(1):300060519859752. doi: 10.1177/0300060519859752. Epub 2019 Jul 15. J Int Med Res. 2020. PMID: 31304847 Free PMC article.

2

Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.

Mao J, Wang T, Wang BJ, Liu YH, Li H, Zhang J, Cram D, Chen Y. Mao J, et al. Among authors: liu yh. Clin Chim Acta. 2014 Jun 10;433:190-3. doi: 10.1016/j.cca.2014.03.011. Epub 2014 Mar 22. Clin Chim Acta. 2014. PMID: 24667696

3

Submicroscopic chromosomal imbalances contribute to early abortion.

Li H, Liu M, Xie M, Zhang Q, Xiang J, Duan C, Ding Y, Liu Y, Mao J, Wang T, Li H. Li H, et al. Among authors: liu y, liu m. Mol Cytogenet. 2018 Jul 21;11:41. doi: 10.1186/s13039-018-0386-0. eCollection 2018. Mol Cytogenet. 2018. PMID: 30038665 Free PMC article.

4

Trophoblast-derived hyaluronan promotes the regulatory phenotype of decidual macrophages.

Wang S, Sun F, Han M, Liu Y, Zou Q, Wang F, Tao Y, Li D, Du M, Li H, Zhu R. Wang S, et al. Among authors: liu y. Reproduction. 2019 Feb 1;157(2):189-198. doi: 10.1530/REP-18-0450. Reproduction. 2019. PMID: 30605433

5

Two heterozygous mutations in the ERCC6 gene associated with Cockayne syndrome in a Chinese patient.

Zhang Q, Liu M, Liu Y, Tang H, Wang T, Li H, Xiang J. Zhang Q, et al. Among authors: liu y, liu m. J Int Med Res. 2020 Feb;48(2):300060519877997. doi: 10.1177/0300060519877997. Epub 2019 Sep 26. J Int Med Res. 2020. PMID: 31558084 Free PMC article.

6

Experimental factors are associated with fetal fraction in size selection noninvasive prenatal testing.

Qiao L, Mao J, Liu M, Liu Y, Song X, Tang H, Zhang Q, Li H, Lu Y, Liang Y, Wang T. Qiao L, et al. Among authors: liu y, liu m. Am J Transl Res. 2019 Oct 15;11(10):6370-6381. eCollection 2019. Am J Transl Res. 2019. PMID: 31737189 Free PMC article.

7

[Clinical and genetic analysis of a child with chromosomal 13q32.1-q33.3 deletion].

Wang H, Huang C, Li L, Liu Y, Wang T, Zhang Y, Li H. Wang H, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Dec 10;36(12):1213-1218. doi: 10.3760/cma.j.issn.1003-9406.2019.12.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31813151 Chinese.

8

[Prenatal diagnosis of a fetus with cleft lip and palate by using chromosomal microarray analysis].

Huang C, Song X, Zhang Q, Liu M, Mao J, Xiang J, Liu Y, Li H, Wang T. Huang C, et al. Among authors: liu y, liu m. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Apr 10;37(4):471-474. doi: 10.3760/cma.j.issn.1003-9406.2020.04.027. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32219840 Chinese.

9

Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 Pregnancies.

Xiang J, Ding Y, Song X, Mao J, Liu M, Liu Y, Huang C, Zhang Q, Wang T. Xiang J, et al. Among authors: liu y, liu m. Front Genet. 2020 Nov 6;11:571219. doi: 10.3389/fgene.2020.571219. eCollection 2020. Front Genet. 2020. PMID: 33240322 Free PMC article.

10

[Whole exome sequencing analysis and prenatal diagnosis for a Chinese pedigree affected with microphthalmia].

Zhang Q, Xiang J, Yang F, Zhang W, Mao J, Liu Y, Li H. Zhang Q, et al. Among authors: liu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jan 10;38(1):56-58. doi: 10.3760/cma.j.cn511374-20190829-00438. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33423259 Chinese.

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