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S M Forrest

Showing results (31-40 of 48) with videos related to

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Journal of Medical Genetics|September 11, 1998
Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA geneM B Delatycki, D Paris, R J Gardner, et al.
Neurology|November 28, 2001
A new autosomal dominant pure cerebellar ataxiaE Storey, R J Gardner, M A Knight, et al.
Journal of Medical Genetics|December 24, 1998
Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctataL J Sheffield, A H Osborn, W M Hutchison, et al.
Neurogenetics|March 25, 2000
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA geneS M Forrest, M Knight, M B Delatycki, et al.
The EMBO Journal|November 1, 1987
Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patientsG S Cross, A Speer, A Rosenthal, et al.
American Journal of Medical Genetics|February 24, 2001
Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxiaE Storey, D du Sart, J H Shaw, et al.
Calcified Tissue International|January 1, 1985
Characterization of an osteoblast-like clonal cell line which responds to both parathyroid hormone and calcitoninS M Forrest, K W Ng, D M Findlay, et al.
Journal of Muscle Research and Cell Motility|February 1, 1988
Molecular analysis of muscular dystrophyK E Davies, S J Kenwrick, M N Patterson, et al.
American Journal of Human Genetics|April 1, 1997
X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26M Lagerström-Fermér, M Sundvall, E Johnsen, et al.
Lancet (London, England)|November 28, 1992
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|September 11, 1998
Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA geneM B Delatycki, D Paris, R J Gardner, et al.
Neurology|November 28, 2001
A new autosomal dominant pure cerebellar ataxiaE Storey, R J Gardner, M A Knight, et al.
Journal of Medical Genetics|December 24, 1998
Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctataL J Sheffield, A H Osborn, W M Hutchison, et al.
Neurogenetics|March 25, 2000
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA geneS M Forrest, M Knight, M B Delatycki, et al.
The EMBO Journal|November 1, 1987
Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patientsG S Cross, A Speer, A Rosenthal, et al.
American Journal of Medical Genetics|February 24, 2001
Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxiaE Storey, D du Sart, J H Shaw, et al.
Calcified Tissue International|January 1, 1985
Characterization of an osteoblast-like clonal cell line which responds to both parathyroid hormone and calcitoninS M Forrest, K W Ng, D M Findlay, et al.
Journal of Muscle Research and Cell Motility|February 1, 1988
Molecular analysis of muscular dystrophyK E Davies, S J Kenwrick, M N Patterson, et al.
American Journal of Human Genetics|April 1, 1997
X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26M Lagerström-Fermér, M Sundvall, E Johnsen, et al.
Lancet (London, England)|November 28, 1992
Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney diseaseD Ravine, R G Walker, R N Gibson, et al.
Pageof 5