Wang HY - Search Results

1

[Clinical and experimental studies of childhood acute myeloid leukemia with 11q23/MLL rearrangements].

He YX, Xue YQ, Wang HY, Shao XJ, Pan JL, Xu J, Yang NC, Ji ZH, Huang YP, Hu SY. He YX, et al. Among authors: wang hy. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):677-82. doi: 10.3760/cma.j.issn.1003-9406.2012.06.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23225048 Chinese.

2

[Clinical and laboratory features of pediatric acute myeloid leukemia with inversion of chromosome 16].

He YX, Xue YQ, Wang HY, Yang NC, Shao XJ, Xu J, Ji ZH, Huang YP, Ding YF, Hu SY. He YX, et al. Among authors: wang hy. Zhonghua Er Ke Za Zhi. 2012 Aug;50(8):593-7. Zhonghua Er Ke Za Zhi. 2012. PMID: 23158736 Chinese.

3

[Genetic analysis of three children with disorders of sex development caused by structural rearrangements of Y chromosome].

Wang H, Chen L, Chen Y, Shen Y, Li L, Shao X, Li H. Wang H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Nov 10;37(11):1226-1232. doi: 10.3760/cma.j.cn511374-20190725-00373. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 33179226 Chinese.

4

The clinical analysis of small supernumerary marker chromosomes in 17 children with mos 45,X/46,X,+mar karyotype.

Wang H, Wang T, Yang N, He Y, Chen L, Hong L, Shao X, Li H, Zhu H, Li H. Wang H, et al. Oncol Lett. 2017 Jun;13(6):4385-4389. doi: 10.3892/ol.2017.5965. Epub 2017 Mar 31. Oncol Lett. 2017. PMID: 28588710 Free PMC article.

5

[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. 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.

6

[Advance in clinical research on Antley-Bixler syndrome].

Xie M, Wang H, Chen L, Li H, Li H. Xie M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):280-283. doi: 10.3760/cma.j.issn.1003-9406.2018.02.031. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29653011 Review. Chinese.

7

De novo ATP1A2 variants in two Chinese children with alternating hemiplegia of childhood upgraded the gene-disease relationship and variant classification: a case report.

Huang D, Liu M, Wang H, Zhang B, Zhao D, Ling W, Wang M, Feng J, Shen Y, Chen X. Huang D, et al. BMC Med Genomics. 2021 Apr 1;14(1):95. doi: 10.1186/s12920-021-00947-6. BMC Med Genomics. 2021. PMID: 33794876 Free PMC article.

8

CNV profiles of Chinese pediatric patients with developmental disorders.

Yuan H, Shangguan S, Li Z, Luo J, Su J, Yao R, Zhang S, Liang C, Chen Q, Gao Z, Zhu Y, Zhang S, Li W, Lu W, Zhang Y, Xie H, Liu F, Wang Q, Lin Y, Liu L, Wang X, Liang L, Zhong J, Li H, Qiu H, Zhang H, Yan M, Mireguli M, Liu Y, Zhang D, Wang H, Lv H, Xie B, Gui C, Cui X, Zou L, Wang J, Gusella JF, Shen Y, Chen X. Yuan H, et al. Genet Med. 2021 Apr;23(4):669-678. doi: 10.1038/s41436-020-01048-y. Epub 2021 Jan 5. Genet Med. 2021. PMID: 33402738 Free article.

9

Long-read sequencing identified a novel nonsense and a de novo missense of PPA2 in trans in a Chinese patient with autosomal recessive infantile sudden cardiac failure.

Zhao A, Shen J, Ding Y, Sheng M, Zuo M, Lv H, Wang J, Shen Y, Wang H, Sun L. Zhao A, et al. Clin Chim Acta. 2021 Aug;519:163-171. doi: 10.1016/j.cca.2021.03.029. Epub 2021 Apr 5. Clin Chim Acta. 2021. PMID: 33826954

10

Clinical and Molecular Characteristics of Two Chinese Children with Infantile Sandhoff Disease and Review of the Literature.

Liu M, Huang D, Wang H, Zhao L, Wang Q, Chen X. Liu M, et al. J Mol Neurosci. 2020 Apr;70(4):481-487. doi: 10.1007/s12031-019-01409-6. Epub 2020 Jan 9. J Mol Neurosci. 2020. PMID: 31919734 Review.

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