Zhang H - Search Results

1

Rapid Diagnosis of Imprinting Disorders Involving Copy Number Variation and Uniparental Disomy Using Genome-Wide SNP Microarrays.

Liu W, Zhang R, Wei J, Zhang H, Yu G, Li Z, Chen M, Sun X. Liu W, et al. Among authors: zhang r, zhang h. Cytogenet Genome Res. 2015;146(1):9-18. doi: 10.1159/000435847. Epub 2015 Jul 16. Cytogenet Genome Res. 2015. PMID: 26184742

2

[Clinical practice guidelines for the diagnosis of regions of homozygosity and uniparental disomy].

Zhu L, Zhang H, Li Z, Liu W, Sun X. Zhu L, et al. Among authors: zhang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Nov 10;38(11):1140-1144. doi: 10.3760/cma.j.cn511374-20210303-00178. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34729761 Chinese.

3

[Clinical practice guidelines for the diagnosis of regions of homozygosity and uniparental disomy].

Zhu L, Zhang H, Li Z, Liu W, Sun X. Zhu L, et al. Among authors: zhang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Nov 10;38(11):1140-1144. doi: 10.3760/cma.j.cn511374-20210303-00178. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34839523 Chinese.

4

Implementation of a High-Resolution Single-Nucleotide Polymorphism Array in Analyzing the Products of Conception.

Zhang H, Liu W, Chen M, Li Z, Sun X, Wang C. Zhang H, et al. Genet Test Mol Biomarkers. 2016 Jul;20(7):352-8. doi: 10.1089/gtmb.2016.0035. Epub 2016 May 26. Genet Test Mol Biomarkers. 2016. PMID: 27228077

5

[Analysis of de novo copy number variations in a family affected with autism spectrum disorders using high-resolution array-based comparative genomic hybridization].

He WZ, Liu WQ, Zhong XQ, Chen XL, Li SY, Zhang HM, Li Q, Cui QL, Sun XF. He WZ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Jun;29(3):266-9. doi: 10.3760/cma.j.issn.1003-9406.2012.03.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22678785 Chinese.

6

The performance of MALBAC and MDA methods in the identification of concurrent mutations and aneuploidy screening to diagnose beta-thalassaemia disorders at the single- and multiple-cell levels.

Liu W, Zhang H, Hu D, Lu S, Sun X. Liu W, et al. Among authors: zhang h. J Clin Lab Anal. 2018 Feb;32(2):e22267. doi: 10.1002/jcla.22267. Epub 2017 May 26. J Clin Lab Anal. 2018. PMID: 28548214 Free PMC article.

7

[Comprehensive genetic analysis in first or second trimester pregnancy loss using chromosomal microarray with single nucleotide polymorphism probes].

Zhu L, Zhang H, Du Q, Sun X, Liu W. Zhu L, et al. Among authors: zhang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Jun 10;39(6):576-580. doi: 10.3760/cma.j.cn511374-20210506-00387. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35773758 Chinese.

8

Prenatal diagnosis of complete maternal uniparental isodisomy of chromosome 4 in a fetus without congenital abnormality or inherited disease-associated variations.

Liu W, Zhang H, Wang J, Yu G, Qiu W, Li Z, Chen M, Choy KW, Sun X. Liu W, et al. Among authors: zhang h. Mol Cytogenet. 2015 Nov 4;8:85. doi: 10.1186/s13039-015-0190-z. eCollection 2015. Mol Cytogenet. 2015. PMID: 26539248 Free PMC article.

9

Identification of copy number variants by NGS-based NIPT at low sequencing depth.

Ye X, Lin S, Song X, Tan M, Li J, Wang J, Yan H, Zhang H, Li S, Chen D, Chen M. Ye X, et al. Among authors: zhang h. Eur J Obstet Gynecol Reprod Biol. 2021 Jan;256:297-301. doi: 10.1016/j.ejogrb.2020.11.026. Epub 2020 Nov 11. Eur J Obstet Gynecol Reprod Biol. 2021. PMID: 33310305

10

Prenatal diagnosis of Roberts syndrome in a Chinese family based on ultrasound findings and whole exome sequencing: a case report.

Zhu L, Cao D, Chen M, Zhang H, Sun X, Liu W. Zhu L, et al. Among authors: zhang h. BMC Med Genomics. 2022 Jan 29;15(1):16. doi: 10.1186/s12920-022-01161-8. BMC Med Genomics. 2022. PMID: 35093090 Free PMC article.

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