Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene.

The cloned complementary DNA for coagulation Factor IX (FIX) detects a frequent restriction fragment length polymorphism (RFLP) in human genomic DNAs digested with the restriction endonuclease Taq I. This genetic marker was used, in parallel with coagulation and immunological assays, to follow the s...

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Enregistré dans:
Détails bibliographiques
Publié dans:J Clin Invest
Auteurs principaux: Grunebaum, L, Cazenave, J P, Camerino, G, Kloepfer, C, Mandel, J L, Tolstoshev, P, Jaye, M, De la Salle, H, Lecocq, J P
Format: Artigo
Langue:Inglês
Publié: American Society for Clinical Investigation 1984
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC425173/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6325506/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI111354
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