Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy.

Por van Bakel, I, Holt, S, Craig, I, Boyd, Y
Publicado em 1995

Abnormalities of copper accumulation in cell lines established from nine different alleles of mottled are the same as those found in Menkes disease.

Por Masson, W, Hughes, H, Papworth, D, Boyd, Y, Horn, N
Publicado em 1997

Multi-allelic RFLP for M27 beta, an anonymous single copy genomic clone at Xp11.3-Xcen [HGM9 provisional no. DXS255].

Por Fraser, N J, Boyd, Y, Brownlee, G G, Craig, I W
Publicado em 1987

Muscular dystrophy in girls with X;autosome translocations.

Por Boyd, Y, Buckle, V, Holt, S, Munro, E, Hunter, D, Craig, I
Publicado em 1986

Two RFLPs at the D12S51 locus

Por Newton, R., Henderson, D.J., Cockburn, D.J., Boyd, Y., Moore, G.E.
Publicado em 1991

Duchenne muscular dystrophy in one of monozygotic twin girls.

Por Burn, J, Povey, S, Boyd, Y, Munro, E A, West, L, Harper, K, Thomas, D
Publicado em 1986

Localisation of Y chromosome sequences in normal and 'XX' males.

Por Buckle, V J, Boyd, Y, Fraser, N, Goodfellow, P N, Goodfellow, P J, Wolfe, J, Craig, I W
Publicado em 1987

Molecular and functional characterization of amylin, a peptide associated with type 2 diabetes mellitus.

Por Roberts, A N, Leighton, B, Todd, J A, Cockburn, D, Schofield, P N, Sutton, R, Holt, S, Boyd, Y, Day, A J, Foot, E A
Publicado em 1989