The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

Two DNA recombinant clones, shown by separate studies to contain DNA sequences homologous to the genes coding for the human blood coagulation Factors VIII and IX, were hybridized in situ to metaphases or prometaphases derived from patients with the fragile-X syndrome and from a normal control. The r...

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Detaylı Bibliyografya
Yayımlandı:EMBO J
Asıl Yazarlar: Purrello, M, Alhadeff, B, Esposito, D, Szabo, P, Rocchi, M, Truett, M, Masiarz, F, Siniscalco, M
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 1985
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC554248/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3924593/
https://ncbi.nlm.nih.govhttps://doi.org/10.1002/j.1460-2075.1985.tb03689.x
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