Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family-Reference-Cited by-同舟云学术

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Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family

Published:2017-01-02 Issue:1 Volume:41 Page:68-72
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

He Sheng¹,Qin Qian²,Lin Li¹,Chen Qiuli¹,Yi Shang¹,Wei Honhwei¹,Du Juan¹,Zheng Chenguang¹,Qiu Xiaoxia¹,Chen Biyan¹

Affiliation:

1. Prenatal Diagnostic Center, Guangxi Zhuang Autonomous Region Women and Children Care Hospital, Nanning, Guangxi, People’s Republic of China;

2. Prenatal Diagnostic Center, Baise Women and Children Care Hospital, Baise, Guangxi, People’s Republic of China

Funder

Natural Science Foundation of China

Natural Science Foundation of Guangxi

Guangxi Science and Technology Project

Health Department of Guangxi Province

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2017.1295985

Reference16 articles.

1. Hb Cervantes, Hb Marañón, Hb La Mancha and Hb Goya: Description of 4 new haemoglobinopathies

2. Hemoglobinopathies Worldwide: Present and Future

3. Structural and Functional Characterization of a New Double Variant Haemoglobin (HbG-Philadelphia/Duarte α268Asn→Lysβ262Ala→Pro)

4. Prevalence and molecular characterization of abnormal hemoglobin in eastern Guangdong of southern China

5. Prevalence and Molecular Characterization of Structural Hemoglobin Variants in the Dongguan Region of Guangdong Province, Southern China

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1. The population incidence of thalassemia gene variants in Baise, Guangxi, P. R. China, based on random samples;Hematology;2022-09-06

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