The prevalence and molecular characterization of (δβ)0-thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang population-Reference-Cited by-同舟云学术

The prevalence and molecular characterization of (δβ)0-thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang population

Published:2017-08-01 Issue:3 Volume:32 Page:e22304
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

He Sheng¹,Wei Yuan¹,Lin Li¹,Chen Qiuli¹,Yi Shang¹,Zuo Yangjin¹,Wei Hongwei¹,Zheng Chenguang¹,Chen Biyan¹,Qiu XiaoXia¹^ORCID

Affiliation:

1. Prenatal Diagnosis Center; Guangxi Zhuang Autonomous Region Women and Children Care Hospital; Nanning China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangxi Province

Guangxi Science and Technology Project

Department of Health of Guangdong Province

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Reference34 articles.

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4. Identification of rare and novel deletions that cause (δβ)0-thal and hereditary persistence of foetal haemoglobin in Indian population;Mayuranathan;Eur J Haematol,2014

5. Fetal hemoglobin levels in adults;Rochette;Blood Rev,1994

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