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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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Hlavní autoři: Grunebaum, L, Cazenave, J P, Camerino, G, Kloepfer, C, Mandel, J L, Tolstoshev, P, Jaye, M, De la Salle, H, Lecocq, J P
Médium: Artigo
Jazyk:Inglês
Vydáno: 1984
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC425173/
https://ncbi.nlm.nih.gov/pubmed/6325506
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