Hao N - Search Results

1

Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid.

Qi Q, Lu S, Zhou X, Yao F, Hao N, Yin G, Li W, Bai J, Li N, Cram DS. Qi Q, et al. Among authors: hao n. Prenat Diagn. 2016 Jun;36(6):576-83. doi: 10.1002/pd.4830. Epub 2016 May 17. Prenat Diagn. 2016. PMID: 27084671

2

A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal Samples.

Zhou X, Chen X, Jiang Y, Qi Q, Hao N, Liu C, Xu M, Cram DS, Liu J. Zhou X, et al. Among authors: hao n. Life (Basel). 2021 Jan 28;11(2):98. doi: 10.3390/life11020098. Life (Basel). 2021. PMID: 33525582 Free PMC article.

3

[Impact of maternal X chromosome aneuploidies on cell free DNA prenatal screening].

Chang JZ, Qi QW, Zhou XY, Jiang YL, Hao N, Zhou J, Li MM, Tian XT, Liu JT. Chang JZ, et al. Among authors: hao n. Zhonghua Fu Chan Ke Za Zhi. 2020 Feb 25;55(2):100-105. doi: 10.3760/cma.j.issn.0529-567X.2020.02.008. Zhonghua Fu Chan Ke Za Zhi. 2020. PMID: 32146738 Chinese.

4

[Establishment of multiple quantitative fluorescent polymerase chain reaction assay and its application in rapid prenatal diagnosis of common chromosome aneuploidies].

Xu AQ, Bian XM, Liu JT, Yao FX, Zhang WM, Hao N, Zhou J. Xu AQ, et al. Among authors: hao n. Zhonghua Fu Chan Ke Za Zhi. 2010 Jul;45(7):481-7. Zhonghua Fu Chan Ke Za Zhi. 2010. PMID: 21029597 Chinese.

5

Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.

Qi Q, Jiang Y, Zhou X, Meng H, Hao N, Chang J, Bai J, Wang C, Wang M, Guo J, Ouyang Y, Xu Z, Xiao M, Zhang VW, Liu J. Qi Q, et al. Among authors: hao n. Genes (Basel). 2020 Nov 25;11(12):1397. doi: 10.3390/genes11121397. Genes (Basel). 2020. PMID: 33255631 Free PMC article.

6

Factors associated with test failure in pregnant women undergoing cell-free DNA-based testing for fetal trisomy.

Chang J, Qi Q, Zhou X, Jiang Y, Hao N, Liu J. Chang J, et al. Among authors: hao n. J Med Screen. 2021 Dec;28(4):411-418. doi: 10.1177/09691413211009940. Epub 2021 Apr 22. J Med Screen. 2021. PMID: 33884933

7

[Application of the fluorescent in situ hybridization on the prenatal diagnosis of the fetal aneuploidy in the uncultured amniocytes].

Qi Q, Sun N, Hao N. Qi Q, et al. Among authors: hao n. Zhonghua Fu Chan Ke Za Zhi. 2000 Sep;35(9):517-9. Zhonghua Fu Chan Ke Za Zhi. 2000. PMID: 11775938 Chinese.

8

[Prenatal diagnosis of 17q12 microdeletion syndrome in fetal renal abnormalities].

Jiang YL, Qi QW, Zhou XY, Geng FF, Bai JJ, Hao N, Liu JT. Jiang YL, et al. Among authors: hao n. Zhonghua Fu Chan Ke Za Zhi. 2017 Oct 25;52(10):662-668. doi: 10.3760/cma.j.issn.0529-567X.2017.10.004. Zhonghua Fu Chan Ke Za Zhi. 2017. PMID: 29060963 Chinese.

9

A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization.

Qi Q, Zhou X, Jiang Y, Hao N, Zhou J, Zhang L. Qi Q, et al. Among authors: hao n. Mol Cytogenet. 2013 Mar 6;6(1):11. doi: 10.1186/1755-8166-6-11. Mol Cytogenet. 2013. PMID: 23497671 Free PMC article.

10

[Prenatal diagnosis and clinical management of a twin pregnancy consisting of a complete mole and coexisting fetus].

Qi QW, Xiang Y, Hao N, Liu JT, Xu YH, Yang XY, Sun NH. Qi QW, et al. Among authors: hao n. Zhonghua Fu Chan Ke Za Zhi. 2003 Oct;38(10):595-8. Zhonghua Fu Chan Ke Za Zhi. 2003. PMID: 14728860 Chinese.

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