Double Heterozygosity for the Codon β 39 C-to-T Nonsense Mutation and a Triplicate α-Globin Gene Locus Can Cause "Dominantly" Inherited β-Thalassemia Intermedia-Reference-Cited by-同舟云学术

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Double Heterozygosity for the Codon β 39 C-to-T Nonsense Mutation and a Triplicate α-Globin Gene Locus Can Cause "Dominantly" Inherited β-Thalassemia Intermedia

Published:1999-05 Issue:5 Volume:317 Page:341-345
ISSN:0002-9629
Container-title:The American Journal of the Medical Sciences
language:en
Short-container-title:The American Journal of the Medical Sciences

Author:

Rhodes S.L.,Plonczynski M.,Harrell A.,Li J.,Safaya S.,Files J.C.,Steinberg M.H.

Publisher

Elsevier BV

Subject

General Medicine

Reference34 articles.

1. The thalassemias;Weatherall,1994

2. Laboratory detection of hemoglobinopathies and thalassemias;Steinberg,1995

3. Construction of human gene libraries from small amounts of peripheral blood: analysis of beta-like globin genes;Poncz;Hemoglobin,1982

4. Detection of specific sequences among DNA fragments separated by gel electrophoresis;Southern;J Mol Biol,1975

5. DNA sequencing with chain terminating inhibitors;Sanger;Proc Natl Acad Sci USA,1977

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