Mapping of rare X-linked becker muscular dystrophy through double crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids

Por Roncuzzi, L., Fadda, S., Mochi, M., Prosperi, L., Sangiorgi, S., Santamaria, R., Sbarra, D., Besana, D., Morandi, L., Rocchi, M., Romeo, G.
Publicado em 1985

Hereditary thrombophilia: identification of nonsense and missense mutations in the protein C gene.

Por Romeo, G, Hassan, H J, Staempfli, S, Roncuzzi, L, Cianetti, L, Leonardi, A, Vicente, V, Mannucci, P M, Bertina, R, Peschle, C
Publicado em 1987