Severe inclusion body β-thalassaemia with haemolysis in a patient double heterozygous for β°-thalassaemia and quadruplicated α-globin gene arrangement of the anti-4.2 type
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1999.01451.x/fullpdf
Reference20 articles.
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2. Interaction of the heterozygous β°-thalassaemia and triplicated alpha globin loci in a Swiss-Spanish family;Beris;Klinische Wochenschrift,1991
3. De novo initiation codon mutation (ATG → ACG) of the β-globin gene causing β-thalassaemia in a Swiss family;Beris;American Journal of Hematology,1993
4. Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction;Chomczynski;Analytical Biochemistry,1987
5. The rare α-thalassaemia of blacks is a ζ-α-thalassaemia-1 associated with deletion of all α and ζ globin genes;Felice;Blood,1984
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