Alpha thalassaemia in Sardinian newborns
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1984.tb06095.x/fullpdf
Reference29 articles.
1. Beta-Thalassaemia Trait: Imprecision of Diagnosis at Birth
2. Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.
3. Diagnosis of the β0Thalassemia Trait at Birth
4. DIAGNOSIS OF BETA THALASSAEMIA IN THE NEWBORN BY MEANS OF HAEMOGLOBIN SYNTHESIS
5. Haematological characteristics of the beta 0 thalassaemia trait in Sardinian children.
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1. Codon 24 (TAT>TAG) and Codon 32 (ATG>AGG) (Hb Rotterdam): Two Novel α2 Gene Mutations Associated with Mild α-Thalassemia Found in the Same Family After Newborn Screening;Hemoglobin;2010-07-19
2. α-Thalassaemia in Tunisia: some epidemiological and molecular data;Journal of Genetics;2008-09-24
3. alpha-thalassemia carrier identification by DNA analysis in the screening for thalassemia;AM J HEMATOL;1998
4. α-thalassemia carrier identification by DNA analysis in the screening for thalassemia;American Journal of Hematology;1998-12
5. Different Genome Organization in Two New Cell Lines Established from Human Gastric Carcinoma;Cancer Genetics and Cytogenetics;1998-09
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