Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and − −SEA/αα-Reference-Cited by-同舟云学术

Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and − −SEA/αα

Published:2017-05-04 Issue:3 Volume:41 Page:189-192
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Zhang Qiang¹²,Fan Xin²,Xu Mingli¹,Zhang Yijia¹,Xu Huiling¹,Wen Xiaojun¹,Zhou Wanjun¹

Affiliation:

1. Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong Province, People’s Republic of China;

2. Department of Genetic Metabolism, Prenatal Diagnostic Center, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi Zhuang Autonomous Region, People’s Republic of China

Funder

Guangxi Science and Technology Department

Health Department of Guangxi Province

Natural Science Foundation of China

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2017.1366917

Reference18 articles.

1. Prevalence and spectrum of thalassaemia in Changsha, Hunan province, China: discussion of an innovative screening strategy

2. Complexity of the alpha-globin genotypes identified with thalassemia screening in Sardinia

3. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China

4. Rapid diagnosis of alpha-thalassemia-1 of southeast Asia type and hydrops fetalis by polymerase chain reaction [letter]

5. Robot Printing of Reverse Dot Blot Arrays for Human Mutation Detection

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