Molecular, haematological and clinical studies of the −101 C → T substitution of the β-globin gene promoter in 25 β-thalassaemia intermedia patients and 45 heterozygotes
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1999.01788.x/fullpdf
Reference43 articles.
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2. A benign form of thalassaemia intermedia may be determined by the interaction of triplicated α locus and heterozygous β-thalassaemia;Camaschella;British Journal of Haematology,1987
3. Clegg , J.B. 1983 Methods in Haematology: The Thalassaemias 54 73
4. Three regions upstream from the cap site are required for efficient and accurate transcription of the rabbit β-globin gene in mouse 3TG;Dierks;Cell,1983
5. Detecting multiple cystic fibrosis mutations by polymerase chain reaction-mediated site-directed mutagenesis;Friedman;Clinical Chemistry,1991
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