Detection of polymorphisms at cytosine phosphoguanadine dinucleotides and diagnosis of haemophilia B carriers

The polymerase chain reaction procedure (PCR) was used to detect a polymorphic Hha I site adjacent to the factor IX locus in a panel of 33 phenotypically normal caucasian individuals. This technique was also applied to a haemophilia B family pedigree. The Hha I polymorphic site was located 8 kb 3�...

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Veröffentlicht in:The Lancet (British edition) 1989-03, Vol.1 (8639), p.631-634
Hauptverfasser: WINSHIP, P. R, REES, D. J. G, ALKAN, M
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Sprache:eng
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