A substitution of cytosine for thymine in codon 110 of the human ?-globin gene is a novel cause of ?-thalassemia phenotypes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00451448.pdf
Reference31 articles.
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3. Benton WD, Davis RW (1977) Screening ?gt recombinant clones by hybridization to single plaques in situ. Science 196:180?182
4. Bunn HF, Forget BG (1986) Hemoglobin: molecular, genetic and clinical aspects. Saunders, Philadelphia London Tokyo, pp 223?321
5. Carrell RW, Kay R (1972) A simple method for the detection of unstable haemoglobins. Br J Haematol 23:615?619
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1. Hemoglobin Showa-Yakushiji: A Common β Thalassemia Mutation Among the Agri Community from Western India;Genetic Testing and Molecular Biomarkers;2012-04
2. The Rare Hb Showa-Yakushiji [β110(G12)Leu→Pro, CTG→CCG] in Combination with an α Gene Triplication Found in a Dutch Patient During Her First Pregnancy Examination;Hemoglobin;2007-01
3. Dominant β-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the β-globin gene;British Journal of Haematology;1991-10
4. Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms;Cytogenetic and Genome Research;1991
5. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms;Cytogenetic and Genome Research;1990
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