Zhang H - Search Results

1

Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta-analysis.

Zhang Y, Liu Y, Zarrei M, Tong W, Dong R, Wang Y, Zhang H, Yang X, MacDonald JR, Uddin M, Scherer SW, Gai Z. Zhang Y, et al. Among authors: zhang h. Am J Med Genet B Neuropsychiatr Genet. 2018 Jan;177(1):93-100. doi: 10.1002/ajmg.b.32608. Epub 2017 Nov 20. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 29152845

2

Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome.

Zhang K, Liu S, Feng B, Yang Y, Zhang H, Dong R, Liu Y, Gai Z. Zhang K, et al. Among authors: zhang h. PLoS One. 2016 Feb 3;11(2):e0147824. doi: 10.1371/journal.pone.0147824. eCollection 2016. PLoS One. 2016. PMID: 26841067 Free PMC article.

3

Evaluation of High Resolution Melting for MTHFR C677T Genotyping in Congenital Heart Disease.

Wang Y, Zhang H, Yue S, Zhang K, Wang H, Dong R, Yang X, Liu Y, Ma Y. Wang Y, et al. Among authors: zhang k, zhang h. PLoS One. 2016 Mar 18;11(3):e0151140. doi: 10.1371/journal.pone.0151140. eCollection 2016. PLoS One. 2016. PMID: 26990189 Free PMC article. Clinical Trial.

4

Chromosome r(3)(p25.3q29) in a Patient with Developmental Delay and Congenital Heart Defects: A Case Report and a Brief Literature Review.

Zhang K, Song F, Zhang D, Liu Y, Zhang H, Wang Y, Dong R, Zhang Y, Liu Y, Gai Z. Zhang K, et al. Among authors: zhang d, zhang h, zhang y. Cytogenet Genome Res. 2016;148(1):6-13. doi: 10.1159/000445273. Epub 2016 Apr 15. Cytogenet Genome Res. 2016. PMID: 27077748 Review.

5

[Genetic analysis of a child with XYY syndrome mainly featuring mental retardation].

Liu Y, Dong R, Zhang K, Wang Y, Zhang H, Zhang Y, Zhao D, Gai Z. Liu Y, et al. Among authors: zhang k, zhang h, zhang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Oct;33(5):686-9. doi: 10.3760/cma.j.issn.1003-9406.2016.05.024. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27577224 Chinese.

6

Angiopoietin-1 Modified Human Umbilical Cord Mesenchymal Stem Cell Therapy for Endotoxin-Induced Acute Lung Injury in Rats.

Huang ZW, Liu N, Li D, Zhang HY, Wang Y, Liu Y, Zhang LL, Ju XL. Huang ZW, et al. Yonsei Med J. 2017 Jan;58(1):206-216. doi: 10.3349/ymj.2017.58.1.206. Yonsei Med J. 2017. PMID: 27873515 Free PMC article.

7

[Molecular cytogenetic analysis of a case with ring chromosome 3 syndrome].

Zhang K, Song F, Zhang D, Zhang H, Wang Y, Dong R, Zhang Y, Liu Y, Gai Z. Zhang K, et al. Among authors: zhang d, zhang h, zhang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Dec 10;33(6):816-819. doi: 10.3760/cma.j.issn.1003-9406.2016.06.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27984612 Chinese.

8

[Clinical and molecular cytogenetic analysis of a family with mental retardation caused by an unbalanced translocation involving chromosomes 3 and 22].

Zhang K, Dong R, Huang Y, Yang Y, Wang Y, Zhang H, Zhang Y, Liu Y, Gai Z. Zhang K, et al. Among authors: zhang h, zhang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Feb 10;34(1):30-34. doi: 10.3760/cma.j.issn.1003-9406.2017.01.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28186589 Chinese.

9

[Analysis of genetic etiology of a female with 47,XXY syndrome].

Li H, Zhang K, Gao M, Zhang H, Wang Y, Zhang Y, Liu Y, Gai Z. Li H, et al. Among authors: zhang k, zhang h, zhang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Feb 10;34(1):102-105. doi: 10.3760/cma.j.issn.1003-9406.2017.01.024. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28186606 Chinese.

10

Familial intellectual disability as a result of a derivative chromosome 22 originating from a balanced translocation (3;22) in a four generation family.

Zhang K, Huang Y, Dong R, Yang Y, Wang Y, Zhang H, Zhang Y, Gai Z, Liu Y. Zhang K, et al. Among authors: zhang h, zhang y. Mol Cytogenet. 2018 Feb 20;11:18. doi: 10.1186/s13039-017-0349-x. eCollection 2018. Mol Cytogenet. 2018. PMID: 29467824 Free PMC article.

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