| Literature DB >> 8103502 |
G W Hall1, M Sampietro, R Barnetson, J Fitzgerald, S McCann, S L Thein.
Abstract
Using the technique of allele-specific priming of the polymerase chain reaction (PCR), the C-T substitution in codon 39 was identified as the cause of beta-thalassaemia in an Irish family. Analysis of the restriction fragment length polymorphisms (RFLPs) in the beta-globin gene cluster established linkage of the beta-thalassaemia mutation to a particular beta-haplotype but indicated that a recombinational event had occurred in the paternal chromosome in the younger of two affected children. Non-paternity was excluded by DNA fingerprinting analysis with hypervariable minisatellite probes. This is the fourth case of recombination in the beta-globin gene cluster to be reported. The event has occurred 5' of the polymorphic RsaI site at position -550 bp upstream of the beta-globin gene mRNA Cap site, within the 9.1-kb region that has been shown to be a hot spot for recombination in the beta-globin gene cluster.Entities:
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Year: 1993 PMID: 8103502 DOI: 10.1007/bf00216141
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132