Thalassemia Intermedia Due to Co‐inheritance of β0/β+‐Thalassemia and (– –SEA)α‐Thalassemia/Hb Westmead [α122(H5)His > Gln (α2)] in a Chinese Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1081/HEM-120035917
Reference11 articles.
1. Prevalence and Genotypes of α- and β-Thalassemia Carriers in Hong Kong — Implications for Population Screening
2. The β-Thalassemias
3. Hemoglobin Westmead α2122(H5)His←Glnβ2: A New Hemoglobin Variant with the Substitution in the α1β1Contact Area
4. Hb Westmead: An α2-Globin Gene Mutation Detected by Polymerase Chain Reaction and STU I Cleavage
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