Li H - Search Results

1

Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.

Mao J, Wang T, Wang BJ, Liu YH, Li H, Zhang J, Cram D, Chen Y. Mao J, et al. Among authors: li h. Clin Chim Acta. 2014 Jun 10;433:190-3. doi: 10.1016/j.cca.2014.03.011. Epub 2014 Mar 22. Clin Chim Acta. 2014. PMID: 24667696

2

[A pedigree with blepharophimosis-ptosis-epicanthus inversus syndrome].

Cheng H, Yang N, Liu J, Song L, Wang T, Lin LQ, Xu Q, Yang S, Shen L, Song D, Wang T, Wang W, Shi Y, Li H. Cheng H, et al. Among authors: li h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Jun;30(3):382. doi: 10.3760/cma.j.issn.1003-9406.2013.03.032. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23744336 Chinese. No abstract available.

3

[Non-syndromic autosomal dominant type deafness: report of a family with 26 cases].

Liu JZ, Cheng HB, Yang N, Lin LQ, Xu QY, Gu X, Shi YC, Yang SM, Shen LY, Song D, Wang T, Wang W, Li Q, Li H. Liu JZ, et al. Among authors: li h, li q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Aug;30(4):501. doi: 10.3760/cma.j.issn.1003-9406.2013.04.025. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23926024 Chinese. No abstract available.

4

A patient with five chromosomal rearrangements and a 2q31.1 microdeletion.

Wang T, Mao J, Liu MJ, Choy KW, Li HB, Cram DS, Li H, Chen Y. Wang T, et al. Among authors: li h, li hb. Clin Chim Acta. 2014 Mar 20;430:129-33. doi: 10.1016/j.cca.2014.01.002. Epub 2014 Jan 9. Clin Chim Acta. 2014. PMID: 24412318

5

[A microdeletion of chromosome 9q34.11 may cause suspected cerebral palsy].

Li H, Chen Y, Li Q, Liu M, Mao J, Song D, Li H. Li H, et al. Among authors: li q. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):725-9. doi: 10.3760/cma.j.issn.1003-9406.2014.06.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449075 Chinese.

6

SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes.

Li H, Wang B, Liu D, Wang T, Li Q, Wang W, Li H. Li H, et al. Among authors: li q. Genomics. 2015 Aug;106(2):83-7. doi: 10.1016/j.ygeno.2015.05.004. Epub 2015 May 22. Genomics. 2015. PMID: 26004784 Free article.

7

Prenatal Diagnosis and Genetic Analysis of a Fetus with Joubert Syndrome.

Xiang J, Zhang L, Jiang W, Zhang Q, Wang T, Li H, Li H. Xiang J, et al. Among authors: li h. Biomed Res Int. 2018 May 31;2018:7202168. doi: 10.1155/2018/7202168. eCollection 2018. Biomed Res Int. 2018. PMID: 29955609 Free PMC article.

8

Submicroscopic chromosomal imbalances contribute to early abortion.

Li H, Liu M, Xie M, Zhang Q, Xiang J, Duan C, Ding Y, Liu Y, Mao J, Wang T, Li H. Li H, et al. Mol Cytogenet. 2018 Jul 21;11:41. doi: 10.1186/s13039-018-0386-0. eCollection 2018. Mol Cytogenet. 2018. PMID: 30038665 Free PMC article.

9

CiRS-126 inhibits proliferation of ovarian granulosa cells through targeting the miR-21-PDCD4-ROS axis in a polycystic ovarian syndrome model.

Lu J, Xue Y, Wang Y, Ding Y, Zou Q, Pan M, Qiao L, Zhang C, Ge Q, Wang T, Li H. Lu J, et al. Among authors: li h. Cell Tissue Res. 2020 Jul;381(1):189-201. doi: 10.1007/s00441-020-03187-9. Epub 2020 May 29. Cell Tissue Res. 2020. Retraction in: Cell Tissue Res. 2021 Oct;386(1):213. doi: 10.1007/s00441-021-03484-x. PMID: 32468088 Retracted.

10

[Improved identification for trisomy 9p and partial trisomy 6q presented in a patient by array-based comparative genomic hybridization].

Zhang J, Cai J, Yang Y, Wang S, Yao F, Huang C, Li H, Li H, Zhang Y. Zhang J, et al. Among authors: li h. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Dec 10;33(6):829-832. doi: 10.3760/cma.j.issn.1003-9406.2016.06.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27984615 Chinese.

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