K Morgan

Analysis of 14 CAG repeat-containing genes in schizophrenia.

A Labelle, M. Alda, C. Benkelfat, 1999, American journal of medical genetics.

Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian population.

L. Simard, B. Lemieux, K. Morgan, 1994, Human molecular genetics.

Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.

T. Hudson, A. Verner, G. Mitchell, 2000, American journal of human genetics.

The effect of intragenic recombination on the number of alleles in a finite population.

C. Strobeck, K. Morgan, K Morgan, 1978, Genetics.

Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.

C. Greenberg, T. Weiler, K. Morgan, 1996, American journal of human genetics.