Search research articles
Contact Us
Filters
Showing results (61-70 of 71) with videos related to
Page
of 8
Sort By:
Journal of Medical Genetics
|
March 1, 1995
A gene for familial venous malformations maps to chromosome 9p in a second large kindred
C J Gallione, K A Pasyk, L M Boon, et al.
American Journal of Medical Genetics
|
August 14, 1995
Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia
M C Speer, H M Kingston, R M Boustany, et al.
Annals of Neurology
|
November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13
J M Stajich, J M Gilchrist, F Lennon, et al.
Journal of Medical Genetics
|
December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype
K A McAllister, F Lennon, B Bowles-Biesecker, et al.
Genomics
|
August 1, 1993
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity
K Ben Othmane, L T Middleton, L J Loprest, et al.
Neuromuscular Disorders : NMD
|
December 10, 1997
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation
J M Stajich, J M Gilchrist, F Lennon, et al.
American Journal of Human Genetics
|
February 11, 1999
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7
M C Speer, J M Vance, J M Grubber, et al.
Molecular Vision
|
January 5, 2000
North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysis
K W Small, N Udar, S Yelchits, et al.
Human Heredity
|
August 7, 1998
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families
M C Speer, J M Vance, F Lennon-Graham, et al.
Neurogenetics
|
March 25, 2000
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity
M A Pericak-Vance, M C Speer, F Lennon, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 71) with videos related to
Sort By:
Page
of 8
Journal of Medical Genetics
|
March 1, 1995
A gene for familial venous malformations maps to chromosome 9p in a second large kindred
C J Gallione, K A Pasyk, L M Boon, et al.
American Journal of Medical Genetics
|
August 14, 1995
Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia
M C Speer, H M Kingston, R M Boustany, et al.
Annals of Neurology
|
November 1, 1996
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13
J M Stajich, J M Gilchrist, F Lennon, et al.
Journal of Medical Genetics
|
December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype
K A McAllister, F Lennon, B Bowles-Biesecker, et al.
Genomics
|
August 1, 1993
Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity
K Ben Othmane, L T Middleton, L J Loprest, et al.
Neuromuscular Disorders : NMD
|
December 10, 1997
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation
J M Stajich, J M Gilchrist, F Lennon, et al.
American Journal of Human Genetics
|
February 11, 1999
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7
M C Speer, J M Vance, J M Grubber, et al.
Molecular Vision
|
January 5, 2000
North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysis
K W Small, N Udar, S Yelchits, et al.
Human Heredity
|
August 7, 1998
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families
M C Speer, J M Vance, F Lennon-Graham, et al.
Neurogenetics
|
March 25, 2000
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity
M A Pericak-Vance, M C Speer, F Lennon, et al.
Page
of 8