He S - Search Results

1

A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33.

Wang J, Fu C, Zhang S, Luo J, Ouyang L, Xie B, Sun W, He S, Su J, Hu X, Fei D, Chen R, Fan X, Ou S, Chen S, Shen Y. Wang J, et al. Among authors: he s. Gene. 2016 Dec 5;594(1):59-65. doi: 10.1016/j.gene.2016.08.042. Epub 2016 Aug 31. Gene. 2016. PMID: 27591971

2

Prevention and control of Hb Bart's disease in Guangxi Zhuang Autonomous Region, China.

He S, Zhang Q, Li D, Chen S, Tang Y, Chen Q, Zheng C. He S, et al. Eur J Obstet Gynecol Reprod Biol. 2014 Jul;178:138-41. doi: 10.1016/j.ejogrb.2014.03.034. Epub 2014 Apr 13. Eur J Obstet Gynecol Reprod Biol. 2014. PMID: 24792538

3

[Genotypes of 1 571 cases of Hb H disease in Guangxi area].

Fu C, Chen S, Zhang Q, He S, Wei Y, Chen Q, Tang Y, Zheng C. Fu C, et al. Among authors: he s. Zhonghua Xue Ye Xue Za Zhi. 2014 Aug;35(8):728-31. doi: 10.3760/cma.j.issn.0253-2727.2014.08.013. Zhonghua Xue Ye Xue Za Zhi. 2014. PMID: 25152122 Chinese.

4

[Gene distribution characteristics of deletional α-thalassemia in Guangxi region].

Zhang Q, Fan X, He S, Fu C, Tang Y, Chen Q, Wei Y, Zheng C. Zhang Q, et al. Among authors: he s. Zhonghua Xue Ye Xue Za Zhi. 2014 Oct;35(10):941-3. doi: 10.3760/cma.j.issn.0253-2727.2014.10.015. Zhonghua Xue Ye Xue Za Zhi. 2014. PMID: 25339335 Chinese.

5

Hb H Hydrops Fetalis Syndrome Caused by Association of the - -(SEA) Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family.

He S, Zheng C, Meng D, Chen R, Zhang Q, Tian X, Chen S. He S, et al. Hemoglobin. 2015;39(3):216-9. doi: 10.3109/03630269.2015.1030031. Epub 2015 Apr 21. Hemoglobin. 2015. PMID: 25897478

6

First Detection of a Splice Acceptor Site β-Thalassemia Mutation: IVS-I-130 (HBB: c.93-1G > C) in a Chinese Patient.

He S, Zhang Q, Zheng C, Wei Y, Tang Y, Chen Q, Chen S. He S, et al. Hemoglobin. 2015;39(4):290-1. doi: 10.3109/03630269.2015.1039027. Epub 2015 Jul 16. Hemoglobin. 2015. PMID: 26182339

7

Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern China.

He S, Qin Q, Yi S, Wei Y, Lin L, Chen S, Deng J, Xu X, Zheng C, Chen B. He S, et al. Gene. 2017 Jul 1;619:71-75. doi: 10.1016/j.gene.2016.02.014. Epub 2016 Feb 10. Gene. 2017. PMID: 26877226

8

de novo interstitial deletions at the 11q23.3-q24.2 region.

Su J, Chen R, Luo J, Fan X, Fu C, Wang J, He S, Hu X, Zhang S, Yi S, Chen S, Shen Y. Su J, et al. Among authors: he s. Mol Cytogenet. 2016 May 5;9:39. doi: 10.1186/s13039-016-0247-7. eCollection 2016. Mol Cytogenet. 2016. PMID: 27158264 Free PMC article.

9

Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α⁰-Thalassemia in a Chinese Family.

He S, Qin Q, Huang P, Zhang S, Yi S, Lin L, Zuo Y, Chen Q, Deng J, Zheng C, Chen B. He S, et al. Hemoglobin. 2017 Jul-Nov;41(4-6):297-299. doi: 10.1080/03630269.2017.1366919. Epub 2017 Nov 21. Hemoglobin. 2017. PMID: 29161910

10

Molecular characterization of α- and β-thalassemia in the Yulin region of Southern China.

He S, Li J, Li DM, Yi S, Lu X, Luo Y, Liang Y, Feng C, Chen B, Zheng C, Qiu X. He S, et al. Gene. 2018 May 20;655:61-64. doi: 10.1016/j.gene.2018.02.058. Epub 2018 Feb 23. Gene. 2018. PMID: 29477874

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

14,991 results

Search Page

Filters