K. Morgan

发表

Association between Ag I -CA Alleles and Severity of Autosomal Recessive Proximal Spinal Muscular Atrophy

J. Carpten, J. Mendell, L. Simard, 2007 .

Autosomal recessive spastic ataxia of Charlevoix–Saguenay

T. Hudson, J. Bouchard, D. Brunet, 1998, Neuromuscular Disorders.

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)

T. Hudson, J. Bouchard, J. Mathieu, 1979, Neuromuscular Disorders.

Genetic epidemiology of autosomal recessive spastic ataxia of Charlevoix‐Saguenay in northeastern Quebec

J. Bouchard, J. Mathieu, K. Morgan, 1993, Genetic epidemiology.

An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex.

P. Sluijs, D. Bichet, P. Deen, 1998, The Journal of clinical investigation.

Molecular scanning of the human PPARa gene: association of the L162v mutation with hyperapobetalipoproteinemia.

T. Hudson, J. Després, D. Gaudet, 2000, Journal of lipid research.

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.

C. Greenberg, T. Weiler, K. Morgan, 1998, American journal of human 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.

Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11.

G. Gyapay, T. Hudson, J. Weissenbach, 1999, American journal of human genetics.

Autosomal recessive spastic ataxia of Charlevoix–Saguenay

J. Bouchard, D. Brunet, J. Mathieu, 1998, Neuromuscular Disorders.

X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesis.

M. Gregory, D. Bichet, G. Hendy, 1993, The Journal of clinical investigation.

Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.

T. Hudson, J. Rommens, P. Durie, 2001, American journal of human genetics.

Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy.

J. McPherson, J. Carpten, B. Wirth, 1994, American journal of human genetics.

Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8

T. Hudson, A. Verner, A. Pshezhetsky, 2004, Journal of Medical Genetics.