Zhou S - Search Results

1

Clinical impacts of genome-wide noninvasive prenatal testing for rare autosomal trisomy.

Xiang J, Li R, He J, Wang X, Yao L, Song N, Fu F, Zhou S, Wang J, Gao X, Peng J, Wan J, Hu L, Liu A, Guo Y, Peng C, Liu X, Lin J, Li S, Sun J, Li D, Peng Z, Liao C. Xiang J, et al. Among authors: zhou s. Am J Obstet Gynecol MFM. 2023 Jan;5(1):100790. doi: 10.1016/j.ajogmf.2022.100790. Epub 2022 Oct 29. Am J Obstet Gynecol MFM. 2023. PMID: 36377092

2

[Diagnosis of a fetus with a de novo 16q partial trisomy syndrome].

Hu L, Wang W, Li H, Zhou S, Liu S, Yang M, Bu X, He J. Hu L, et al. Among authors: zhou s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Oct 10;37(10):1084-1086. doi: 10.3760/cma.j.cn511374-20191101-00555. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32924106 Chinese.

3

[Value of chromosomal microarray analysis for the prenatal diagnosis of pregnancy with high risk signaled by non-invasive prenatal testing].

Bu X, Zeng L, Li H, Zhou S, Hu L, He J. Bu X, et al. Among authors: zhou s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jun 10;38(6):541-544. doi: 10.3760/cma.j.cn511374-20200420-00285. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34096021 Chinese.

4

Prenatal diagnosis of complete paternal uniparental isodisomy for chromosome 3: a case report.

Bu X, Li X, Zhou S, Shi L, Jiang X, Peng C, Li H, He J. Bu X, et al. Among authors: zhou s. Mol Cytogenet. 2021 Nov 6;14(1):50. doi: 10.1186/s13039-021-00569-8. Mol Cytogenet. 2021. PMID: 34742342 Free PMC article.

5

[Economic burden of Down syndrome patients and psychological and social discrimination to female caregivers in Changsha, China].

Wang N, Zhou S, Wang S, Kuang Y, Zu Y, Xie R, Yang M, Peng H, Liu J, He J. Wang N, et al. Among authors: zhou s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jan 10;39(1):11-15. doi: 10.3760/cma.j.cn511374-20210512-00404. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 34964958 Chinese.

6

Cell-Free DNA Screening for Sex Chromosome Abnormalities and Pregnancy Outcomes, 2018-2020: A Retrospective Analysis.

Lu Y, Zhou S, Linpeng S, Ding S, Li S, Li Y, Shi L, He J, Liu Y. Lu Y, et al. Among authors: zhou s. J Pers Med. 2022 Jan 4;12(1):48. doi: 10.3390/jpm12010048. J Pers Med. 2022. PMID: 35055363 Free PMC article.

7

Performance characterization of PCR-free whole genome sequencing for clinical diagnosis.

Zhou G, Zhou M, Zeng F, Zhang N, Sun Y, Qiao Z, Guo X, Zhou S, Yun G, Xie J, Wang X, Liu F, Fan C, Wang Y, Fang Z, Tian Z, Dai W, Sun J, Peng Z, Song L. Zhou G, et al. Among authors: zhou s, zhou m. Medicine (Baltimore). 2022 Mar 11;101(10):e28972. doi: 10.1097/MD.0000000000028972. Medicine (Baltimore). 2022. PMID: 35451387 Free PMC article.

8

Prenatal genetic diagnosis of tetrasomy 18p from maternal trisomy 18p: a case report.

Peng C, LinPeng S, Bu X, Jiang X, Hu L, He J, Zhou S. Peng C, et al. Among authors: zhou s. Mol Cytogenet. 2022 Jun 27;15(1):25. doi: 10.1186/s13039-022-00602-4. Mol Cytogenet. 2022. PMID: 35761312 Free PMC article.

9

[Health economic evaluation of four prenatal screening strategies for Down syndrome in Changsha, China].

He J, Wang S, Zhang J, Zhou S, Kuang Y, Ding J, Yang M, Lin J, Ding S, Liu S, Peng H, Wang N, Liu J. He J, et al. Among authors: zhou s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Aug 10;39(8):803-808. doi: 10.3760/cma.j.cn511374-20211030-00864. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35929926 Chinese.

10

A retrospective single-center analysis of prenatal diagnosis and follow-up of 626 chinese patients with positive non-invasive prenatal screening results.

Bu X, Zhou S, Li X, Li S, Li H, Ding S, He J, Linpeng S. Bu X, et al. Among authors: zhou s. Front Genet. 2022 Sep 19;13:965106. doi: 10.3389/fgene.2022.965106. eCollection 2022. Front Genet. 2022. PMID: 36199578 Free PMC article.

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