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M H Abbott

Showing results (1-10 of 17) with videos related to

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Human Mutation|January 1, 1995
Concentration of mutations causing Schmid metaphyseal chondrodysplasia in the C-terminal noncollagenous domain of type X collagenI McIntosh, M H Abbott, C A Francomano
American Journal of Medical Genetics|April 1, 1987
Psychiatric manifestations of homocystinuria due to cystathionine beta-synthase deficiency: prevalence, natural history, and relationship to neurologic impairment and vitamin B6-responsivenessM H Abbott, S E Folstein, H Abbey, et al.
American Journal of Medical Genetics|January 1, 1978
The familial component in longevity--a study of offspring of nonagenarians: III. Intrafamilial studiesM H Abbott, H Abbey, D R Bolling, et al.
Human Molecular Genetics|February 1, 1994
Additional mutations of type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locusI McIntosh, M H Abbott, M L Warman, et al.
Psychological Medicine|August 1, 1983
The association of affective disorder with Huntington's disease in a case series and in familiesS Folstein, M H Abbott, G A Chase, et al.
Journal of Neurogenetics|April 1, 1984
Phenotypic heterogeneity in Huntington diseaseS E Folstein, M H Abbott, M L Franz, et al.
Human Molecular Genetics|October 1, 1993
Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15O C Stine, N Pleasant, M L Franz, et al.
Neurology|April 12, 2006
The association of CAG repeat length with clinical progression in Huntington diseaseA Rosenblatt, K-Y Liang, H Zhou, et al.
JAMA|June 2, 1989
Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington's diseaseJ Brandt, K A Quaid, S E Folstein, et al.
American Journal of Human Genetics|September 1, 1995
Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington diseaseN G Ranen, O C Stine, M H Abbott, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Human Mutation|January 1, 1995
Concentration of mutations causing Schmid metaphyseal chondrodysplasia in the C-terminal noncollagenous domain of type X collagenI McIntosh, M H Abbott, C A Francomano
American Journal of Medical Genetics|April 1, 1987
Psychiatric manifestations of homocystinuria due to cystathionine beta-synthase deficiency: prevalence, natural history, and relationship to neurologic impairment and vitamin B6-responsivenessM H Abbott, S E Folstein, H Abbey, et al.
American Journal of Medical Genetics|January 1, 1978
The familial component in longevity--a study of offspring of nonagenarians: III. Intrafamilial studiesM H Abbott, H Abbey, D R Bolling, et al.
Human Molecular Genetics|February 1, 1994
Additional mutations of type X collagen confirm COL10A1 as the Schmid metaphyseal chondrodysplasia locusI McIntosh, M H Abbott, M L Warman, et al.
Psychological Medicine|August 1, 1983
The association of affective disorder with Huntington's disease in a case series and in familiesS Folstein, M H Abbott, G A Chase, et al.
Journal of Neurogenetics|April 1, 1984
Phenotypic heterogeneity in Huntington diseaseS E Folstein, M H Abbott, M L Franz, et al.
Human Molecular Genetics|October 1, 1993
Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15O C Stine, N Pleasant, M L Franz, et al.
Neurology|April 12, 2006
The association of CAG repeat length with clinical progression in Huntington diseaseA Rosenblatt, K-Y Liang, H Zhou, et al.
JAMA|June 2, 1989
Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington's diseaseJ Brandt, K A Quaid, S E Folstein, et al.
American Journal of Human Genetics|September 1, 1995
Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington diseaseN G Ranen, O C Stine, M H Abbott, et al.
Pageof 2