Wang H - Search Results

1

The first case of a non-infertile female patient with Pitt-Hopkins syndrome.

Li H, Zhang Y, Yu W, Shu L, Mao X, Jia Z, Xi H, Wang H. Li H, et al. Among authors: wang h. Am J Med Genet A. 2019 Nov;179(11):2311-2314. doi: 10.1002/ajmg.a.61325. Epub 2019 Aug 28. Am J Med Genet A. 2019. PMID: 31464085 No abstract available.

2

[Analysis of four fetuses with de novo chromosomal rearrangments using single nucleotide polymorphism microarray chips].

Wang H, Xi H, Jia ZJ, Huang DM, Zhou YC, Wu LQ. Wang H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):658-61. doi: 10.3760/cma.j.issn.1003-9406.2012.06.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23225044 Chinese.

3

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing.

Liang D, Lv W, Wang H, Xu L, Liu J, Li H, Hu L, Peng Y, Wu L. Liang D, et al. Among authors: wang h. Prenat Diagn. 2013 May;33(5):409-15. doi: 10.1002/pd.4033. Epub 2013 Jan 9. Prenat Diagn. 2013. PMID: 23299662

4

[Prenatal genetic diagnosis for two Chinese families affected with oculocutaneous albinism type Ⅱ].

Hu H, Wang H, Jia Z, Xie Q. Hu H, et al. Among authors: wang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):424-7. doi: 10.3760/cma.j.issn.1003-9406.2014.04.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25119903 Chinese.

5

[Prenatal diagnosis of a case of Pallister-Killian syndrome].

Xi H, Wang H, Jia Z, Zhou Y, Yu H, Liu J, Wu L. Xi H, et al. Among authors: wang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):73-6. doi: 10.3760/cma.j.issn.1003-9406.2015.01.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25636105 Chinese.

6

[Application of next-generation DNA sequencing for prenatal testing of fetal chromosomal aneuploidies].

Liu J, Wang H, Xi H, Jia Z, Zhou Y, Wu L. Liu J, et al. Among authors: wang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Aug;32(4):533-7. doi: 10.3760/cma.j.issn.1003-9406.2015.04.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26252102 Chinese.

7

[Genetic analysis for 2 females carrying idic(Y)(p) and with sex development disorders].

Zhang Y, Wang H, Jia Z, Hu J, Cao W, Tan Y. Zhang Y, et al. Among authors: wang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Jun;33(3):335-9. doi: 10.3760/cma.j.issn.1003-9406.2016.03.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27264816 Chinese.

8

A de novo duplication of chromosome 9q34.13-qter in a fetus with Tetralogy of Fallot Syndrome.

Liu J, Hu H, Ma N, Jia Z, Zhou Y, Hu J, Wang H. Liu J, et al. Among authors: wang h. Mol Cytogenet. 2016 Jul 25;9:54. doi: 10.1186/s13039-016-0267-3. eCollection 2016. Mol Cytogenet. 2016. PMID: 27462370 Free PMC article.

9

[Application of single nucleotide polymorphism array for the identification of pathogenic copy number variations in fetuses with malformations and women with an adverse reproductive history].

Liu J, Xi H, Wang H, Jia Z, Zhou Y, Wu L. Liu J, et al. Among authors: wang h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):173-177. doi: 10.3760/cma.j.issn.1003-9406.2017.02.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397212 Chinese.

10

Carnitine-acylcarnitine translocase deficiency with c.199-10 T>G and novel c.1A>G mutation: Two case reports and brief literature review.

Yan HM, Hu H, Ahmed A, Feng BB, Liu J, Jia ZJ, Wang H. Yan HM, et al. Among authors: wang h. Medicine (Baltimore). 2017 Nov;96(45):e8549. doi: 10.1097/MD.0000000000008549. Medicine (Baltimore). 2017. PMID: 29137068 Free PMC article. Review.

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