Molecular analysis of hemoglobinopathies in a large ethnic Hakka population in southern China-Reference-Cited by-同舟云学术

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Molecular analysis of hemoglobinopathies in a large ethnic Hakka population in southern China

Published:2018-11 Issue:45 Volume:97 Page:e13034
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Zhao Pingsen,Wu Heming,Weng Ruiqiang

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference23 articles.

1. alpha thalassemia and beta thalassemia;Gatto;Rass Clin Sci,1963

2. Inherited haemoglobin disorders: an increasing global health problem;Weatherall;Bull World Health Org,2001

3. The thalassemia syndromes;Weatherall;Texas Rep Biol Med,1980

4. Thalassemia;Cohen;Hematol Am Soc Hematol Educ Program,2004

5. Thalassaemia: the long road from bedside to genome;Weatherall;Nat Rev Genet,2004

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1. Molecular Characterization of α‐ and β‐Thalassemia Among Children Less Than 18 Years Old in Guizhou, China;Journal of Clinical Laboratory Analysis;2024-03

2. Prevalence and genetic analysis of triplicated α-globin gene in Ganzhou region using high-throughput sequencing;Frontiers in Genetics;2023-10-19

3. Next-generation sequencing analysis of the molecular spectrum of thalassemia in Southern Jiangxi, China;Human Genomics;2023-08-17

4. Αlpha-thalassemia genotypes in Vietnam: a report of 12,030 pregnant women and their husbands performing prenatal screening for alpha-thalassemia;Medical Journal of Indonesia;2023-07-12

5. The Need for Translational Epidemiology in Beta Thalassemia Syndromes;Hematology/Oncology Clinics of North America;2023-04

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