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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:EMBO J
Glavni autori: Purrello, M, Alhadeff, B, Esposito, D, Szabo, P, Rocchi, M, Truett, M, Masiarz, F, Siniscalco, M
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group 1985
Teme:
Research Article
Online pristup: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
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items