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Presence of gene for β globin in homozygous β0 thalassaemia

Published in: Nature

Date of publication: January 1, 1976

Language: English

Main subject: homozygosity

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Cites articles 12

Date

Title

Authors

August 1, 1966

Abnormal human haemoglobins. Separation and characterization of the alpha and beta chains by chromatography, and the determination of two new variants, hb Chesapeak and hb J (Bangkok)
March 1, 1969

The pattern of disordered haemoglobin synthesis in homozygous and heterozygous beta-thalassaemia
July 1, 1972

Induction of -globin synthesis in the -thalassaemia of Ferrara
August 1, 1972

Controlled fragmentation of DNA by DNase I
October 1, 1974

The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion
October 1, 1974

Genetic lesion in homozygous alpha thalassaemia (hydrops fetalis)
February 1, 1974

Absence of messenger RNA for beta globin chain in beta(0) thalassaemia
April 1, 1974

Kinetic studies of gene frequency. I. Use of a DNA copy of reticulocyte 9 S RNA to estimate globin gene dosage in mouse tissues
May 1, 1975

Deletion of alpha-globin genes in haemoglobin-H disease demonstrates multiple alpha-globin structural loci
August 1, 1975

The α-chain-termination mutants and their relation to the α-thalassaemias
June 1, 1975

Human globin gene analysis for a patient with beta-o/delta beta-thalassemia
January 1, 1975

Human globin gene expression and linkage in bone marrow and fetal liver

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