Identification of Three Types of α-Thalassemia Deletion, –α21.9, –α2.4, and – –THAI, and Their Frequencies, in One Family in the Population of Southern Guangxi Zhuang Autonomous Region, People’s Republic of China-Reference-Cited by-同舟云学术

Identification of Three Types of α-Thalassemia Deletion, –α21.9, –α2.4, and – –THAI, and Their Frequencies, in One Family in the Population of Southern Guangxi Zhuang Autonomous Region, People’s Republic of China

Published:2018-01-02 Issue:1 Volume:42 Page:37-42
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Pang Wanrong¹,Long Ju¹²,Weng Xunjin¹²,Fan Qiongying¹²,Sun Lei¹²,Pan Zhijian¹,Fan Zuqian¹

Affiliation:

1. Laboratory of Medical Genetics, Qinzhou Maternal and Child Health Care Hospital, Qinzhou, Guangxi Zhuang Autonomous Region, People’s Republic of China;

2. Qinzhou Key Laboratory of Molecular and Cell Biology on Endemic Diseases, Qinzhou, Guangxi Zhuang Autonomous Region, People’s Republic of China

Funder

Guangxi Natural Science Foundation

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2018.1428618

Reference14 articles.

1. The diagnosis and molecular analysis of a novel 21.9kb deletion (Qinzhou type deletion) causing α+ thalassemia

2. Diagnosis of a Family with the Novel –α21.9Thalassemia Deletion

3. Identification of the −α2.4Deletion in One Family and in One Hb H Disease Patient in Guangxi, People’s Republic of China

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