Home LiteratureArticle Details
PMID: 2578804 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

(A gamma delta beta)0-Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA.

British journal of haematology ·Vol. 59 ·No. 2 ·1985-02-00 ·Pages 343-56

Henthorn PS, Smithies O, Nakatsuji T, Felice AE, Gardiner MB, Reese AL, Huisman TH

Abstract

DNA from members of 10 Black families with conditions considered to be G gamma (delta beta)0-thalassaemia or G gamma (delta beta)0-HPFH were studied by using restriction enzyme analysis. One or more affected members from each family were shown to have the same deletion of 34 kbp of DNA in the human beta-globin gene cluster. A clone spanning the deletion was isolated from the DNA of one such person and studied in detail. The deletion removed part of the A gamma and all of the psi beta, delta and beta-globin genes and is different from the four previously identified deletions which caused a condition presently known as (A gamma delta beta)0-thalassaemia.

MeSH Terms
Adolescent Adult Blacks Child Chromosome Deletion Chromosome Mapping Cloning, Molecular DNA/genetics DNA Restriction Enzymes Female Fetal Hemoglobin/genetics Globins/genetics Hemoglobinopathies/genetics Humans Male Middle Aged Thalassemia/blood,genetics
Chemicals
Globins DNA Fetal Hemoglobin DNA Restriction Enzymes
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Henthorn P S
Smithies O
Nakatsuji T
Felice A E
Gardiner M B
Reese A L
Huisman T H
Article Info
Journal
British journal of haematology
Abbr.
Br J Haematol
ISSN
0007-1048
Published
1985-02-00
Pages
343-56
Language
English
Region
England
NLM ID
0372544
Subset
IM
Grants
NIADDK NIH HHS · AM 20120 · United States
NIGMS NIH HHS · GM 20069 · United States
NHLBI NIH HHS · HLB-05168 · United States
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