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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Purrello, M, Alhadeff, B, Esposito, D, Szabo, P, Rocchi, M, Truett, M, Masiarz, F, Siniscalco, M
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1985
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC554248/
https://ncbi.nlm.nih.gov/pubmed/3924593
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