Wang H - Search Results

1

Noninvasive prenatal diagnosis of cobalamin C (cblC) deficiency through target region sequencing of cell-free DNA in maternal plasma.

Han L, Chen C, Guo F, Ye J, Peng Z, Qiu W, Wang Y, Li W, Zhang H, Liang L, Wang Y, Wang H, Ji X, Sun J, Gu X. Han L, et al. Among authors: wang h, wang y. Prenat Diagn. 2020 Feb;40(3):324-332. doi: 10.1002/pd.5601. Epub 2019 Dec 26. Prenat Diagn. 2020. PMID: 31697851

2

Prenatal diagnosis of methylmalonic aciduria from amniotic fluid using genetic and biochemical approaches.

Ji X, Wang H, Ye J, Qiu W, Zhang H, Liang L, Xiao B, Dai M, Xu Y, Chen T, Xu F, Chen Y, Ye W, Gu X, Wang L, Han L. Ji X, et al. Among authors: wang h, wang l. Prenat Diagn. 2019 Oct;39(11):993-997. doi: 10.1002/pd.5519. Epub 2019 Aug 5. Prenat Diagn. 2019. PMID: 31278756

3

Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy.

Wang H, Xu Y, Liu X, Wang L, Jiang W, Xiao B, Wei W, Chen Y, Ye W, Ji X. Wang H, et al. Among authors: wang l. Prenat Diagn. 2017 Apr;37(4):356-364. doi: 10.1002/pd.5019. Epub 2017 Mar 6. Prenat Diagn. 2017. PMID: 28181689

4

[Clinical and genetic study of a child with mental retardation and multiple congenital anomalies and a 16p13.11 microdeletion].

Wang H, Xiao B, Ye H, Hu Q, Qiu W. Wang H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Aug;33(4):485-9. doi: 10.3760/cma.j.issn.1003-9406.2016.04.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27455003 Chinese.

5

[Diagnosis of two cases from one family with Joubert syndrome caused by novel mutations of TCTN1 gene by whole exome sequencing].

Wang H, Jiang W, Dai M, Xiao B, Xu Y, Sun Y, Liu Y, Ying X, Sun Y, Wei W, Ji X. Wang H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):686-689. doi: 10.3760/cma.j.issn.1003-9406.2019.07.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302911 Chinese.

6

[Phenotypic and genetic analysis of four patients with 13q33-q34 microdeletion].

Wang H, Xiao B, Ji X, Zhang J, Cao Y, Ni L, Ye H, Shen L. Wang H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Aug 10;34(4):509-513. doi: 10.3760/cma.j.issn.1003-9406.2017.04.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28777848 Chinese.

7

Novel noncontiguous duplications identified with a comprehensive mutation analysis in the DMD gene by DMD gene-targeted sequencing.

Xu Y, Wang H, Xiao B, Wei W, Liu Y, Ye H, Ying X, Chen Y, Liu X, Ji X, Sun Y. Xu Y, et al. Among authors: wang h. Gene. 2018 Mar 1;645:113-118. doi: 10.1016/j.gene.2017.12.037. Epub 2017 Dec 19. Gene. 2018. PMID: 29273555

8

[Phenotypic and genetic analysis of a patient presented with Tietz/Waardenburg type II a syndrome].

Wang H, Tang L, Zhang J, Hu Q, Chen Y, Xiao B. Wang H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Aug;32(4):520-3. doi: 10.3760/cma.j.issn.1003-9406.2015.04.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26252099 Chinese.

9

Flexible progestin-primed ovarian stimulation versus a GnRH antagonist protocol in predicted suboptimal responders undergoing freeze-all cycles: a randomized non-inferiority trial.

Cai H, Shi Z, Liu D, Bai H, Zhou H, Xue X, Li W, Li M, Zhao X, Ma C, Wang H, Wang T, Li N, Wen W, Wang M, Zhang D, Mol BW, Shi J, Tian L. Cai H, et al. Among authors: wang h. Hum Reprod. 2024 Dec 27:deae286. doi: 10.1093/humrep/deae286. Online ahead of print. Hum Reprod. 2024. PMID: 39729571

10

A Case of NTRK Fusion Corpus Sarcoma With Pseudobiphasic Growth Pattern and Literature Review.

Zhang XY, Jiang HW, Wen XB, Yu Q, Li Y, Wang H, Han J, Yang SC. Zhang XY, et al. Among authors: wang h. Int J Gynecol Pathol. 2024 Dec 26. doi: 10.1097/PGP.0000000000001078. Online ahead of print. Int J Gynecol Pathol. 2024. PMID: 39729556

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