L. J. Ward

发表

Linkage studies of Friedreich ataxia by means of blood-group and protein markers.

B. Keats, N. Simpson, S. Krieger, 1987, American journal of human genetics.

PGM1 null allele detected in a Caucasian mother-son pair.

R. Elston, B. Keats, J. Graham, 1985, Human heredity.

Linkage studies of Usher syndrome: analysis of an Acadian kindred in Louisiana.

R. Elston, M. Z. Pelias, A. Wilson, 1988, Cytogenetics and cell genetics.

A linkage study of panic disorder.

R. Elston, R. Noyes, R. Crowe, 1987, Archives of general psychiatry.

Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded.

H. Zoghbi, B. Keats, A. McCall, 1991, American journal of human genetics.

Association between polymorphic blood markers and risk factors for cardiovascular disease in a large pedigree

R. Elston, C. Amos, D. Rao, 1987, Genetic epidemiology.

The Kell blood group locus is close to the cystic fibrosis locus on chromosome 7

J. Weber, B. Keats, L. J. Ward, 1992, Human Genetics.

Gametic equilibrium between 24 polymorphic markers

R. Elston, L. J. Ward, Jaime L. Hernández, 1990, Human Genetics.

Linkage relationships between a major gene for catechol-o-methyltransferase activity and 25 polymorphic marker systems.

R. Elston, R. Weinshilboum, R. Siervogel, 1984, American journal of medical genetics.

"Acadian" and "classical" forms of Friedreich ataxia are most probably caused by mutations at the same locus.

B. Keats, S. Chamberlain, B. Keats, 1989, American journal of medical genetics.