A Double Heterozygote for (δβ)0-Thalassemia and Codons 41/42 (–TTCT) Behaves as a Homozygote for the Frameshift Mutation in a Chinese Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260701459432
Reference3 articles.
1. Prenatal Diagnosis of β-Thalassemia by Reverse Dot-Blot Hybridization in Southern China
2. Molecular characterization of deletional forms of β-thalassemia in Taiwan
3. Screening and genetic diagnosis of haemoglobin disorders
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1. A Novel Method to Identify Autoantibodies against Putative Target Proteins in Serum from beta-Thalassemia Major: A Pilot Study;Biomedicines;2020-04-26
2. Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China;BMC Medical Genetics;2020-02-28
3. Analysis of the Genotypes in a Chinese Population with Increased Hb A2and Low Hematological Indices;Hemoglobin;2018-05-04
4. Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family;Hemoglobin;2017-01-02
5. Screening for common β-globin gene cluster deletions in Chinese individuals with increased hemoglobin F;International Journal of Laboratory Hematology;2015-07-14
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