A comprehensive scanning method for rapid detection of β-globin gene mutations and polymorphisms
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
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1. β‐Thalassemia pathogenic variants in a cohort of children from the East African coast;Molecular Genetics & Genomic Medicine;2020-05-11
2. Compound heterozygosity of a silent beta‐thalassemia mutation at the 3′‐untranslated region ( HBB : c.*132 C>T) and beta‐zero thalassemia results in thalassemia intermedia;Pediatric Blood & Cancer;2020-01-13
3. Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia;International Journal of Laboratory Hematology;2015-09-29
4. Silent β-Thalassemia Mutations at −101 (C>T) and −71 (C>T) and Their Coinheritance with the Sickle Cell Mutation in Bahrain;Hemoglobin;2013-04-15
5. Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areas;Clinica Chimica Acta;2013-01
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