Heterogeneity of DNA deletion in gamma delta beta-thalassemia.
Open Access
- 28 February 1981
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 67 (3), 878-884
- https://doi.org/10.1172/jci110105
Abstract
By restriction endonuclease mapping, gene cloning, and DNA sequencing we have determined the region of DNA that is deleted in a family with gamma delta beta-thalassemia. The deletion removes the linked epsilon, gamma-, and delta-globin structural genes and terminates within the coding portion of the beta-globin gene. Since the extent of DNA deletion in this family differs from that reported in another family, we conclude that gamma delta beta-thalassemia is heterogeneous at the molecular level.This publication has 22 references indexed in Scilit:
- Characterisation of deletions which affect the expression of fetal globin genes in manNature, 1979
- Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia.Proceedings of the National Academy of Sciences, 1979
- Globin gene deletion in HPFH, δ°β° thalassaemia and Hb Lepore diseaseNature, 1979
- Cloning Human Fetal γ Globin and Mouse α-Type Globin DNA: Preparation and Screening of Shotgun CollectionsScience, 1978
- Application of Endonuclease Mapping to the Analysis and Prenatal Diagnosis of Thalassemias Caused by Globin-Gene DeletionNew England Journal of Medicine, 1978
- Changes in restricted human cellular DNA fragments containing globin gene sequences in thalassemias and related disordersProceedings of the National Academy of Sciences, 1978
- Screening λgt Recombinant Clones by Hybridization to Single Plaques in SituScience, 1977
- Charon Phages: Safer Derivatives of Bacteriophage Lambda for DNA CloningScience, 1977
- A new method for sequencing DNA.Proceedings of the National Academy of Sciences, 1977
- Gamma-Beta Thalassemia: A Cause of Hemolytic Disease of the NewbornNew England Journal of Medicine, 1972