Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.

Por Morton, N E, Macpherson, J N
Publicado em 1992

Frequent small amplifications in the FMR-1 gene in fra(X) families: limits to the diagnosis of 'premutations'.

Por Macpherson, J N, Nelson, D L, Jacobs, P A
Publicado em 1992

Extensive Linkage Disequilibrium in the Achaete-Scute Complex of Drosophila Melanogaster

Por Macpherson, J. N., Weir, B. S., Leigh-Brown, A. J.
Publicado em 1990

Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype.

Por Falik-Zaccai, T C, Shachak, E, Yalon, M, Lis, Z, Borochowitz, Z, Macpherson, J N, Nelson, D L, Eichler, E E
Publicado em 1997

Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.

Por Flynn, G A, Hirst, M C, Knight, S J, Macpherson, J N, Barber, J C, Flannery, A V, Davies, K E, Buckle, V J
Publicado em 1993

Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome.

Por Macpherson, J N, Curtis, G, Crolla, J A, Dennis, N, Migeon, B, Grewal, P K, Hirst, M C, Davies, K E, Jacobs, P A
Publicado em 1995

FRAXA and FRAXE: Evidence against segregation distortion and for an effect of intermediate alleles on learning disability

Por Teague, J. W., Morton, N. E., Dennis, N. R., Curtis, G., McKechnie, N., Macpherson, J. N., Murray, A., Pound, M. C., Sharrock, A. J., Youings, S. A., Jacobs, P. A.
Publicado em 1998