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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Detalhes bibliográficos
Publicado no:J Clin Invest
Main Authors: Grunebaum, L, Cazenave, J P, Camerino, G, Kloepfer, C, Mandel, J L, Tolstoshev, P, Jaye, M, De la Salle, H, Lecocq, J P
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 1984
Assuntos:
Research Article
Acesso em linha: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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