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P S Harper

Showing results (181-190 of 345) with videos related to

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Annals of Human Genetics|May 1, 1983
Genetic linkage between the loci for myotonic dystrophy and peptidase DT O'Brien, S Ball, M Sarfarazi, et al.
Community Genetics|February 13, 2004
The frequency of inherited disorders database: prevalence of Huntington diseaseL N Al-Jader, P S Harper, M Krawczak, et al.
Obstetrics and Gynecology|December 1, 1971
George Otto Gey. (1899-1970). The HeLa cell and a reappraisal of its originH W Jones, V A McKusick, P S Harper, et al.
Muscle & Nerve|May 1, 1991
Assessment of locomotor function in young boys with Duchenne muscular dystrophyR A Smith, R G Newcombe, J R Sibert, et al.
Journal of Medical Genetics|December 1, 1986
Molecular deletion analysis in Duchenne muscular dystrophyN S Thomas, P N Ray, R G Worton, et al.
Journal of Medical Genetics|August 1, 1989
A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probesM Upadhyaya, M Sarfarazi, P W Lunt, et al.
Human Molecular Genetics|April 18, 1998
Huntingtin interacts with cystathionine beta-synthaseJ M Boutell, J D Wood, P S Harper, et al.
Human Genetics|April 1, 1987
X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localizationA Clarke, M Sarfarazi, N S Thomas, et al.
Journal of Medical Genetics|December 1, 1982
A clinical and genetic study of Hunter's syndrome. 1. HeterogeneityI D Young, P S Harper, I M Archer, et al.
Lancet (London, England)|September 9, 1989
Problems in genetic prediction for Huntington's diseaseM J Morris, A Tyler, L Lazarou, et al.
Pageof 35

Showing results (181-190 of 345) with videos related to

Sort By:
Pageof 35
Annals of Human Genetics|May 1, 1983
Genetic linkage between the loci for myotonic dystrophy and peptidase DT O'Brien, S Ball, M Sarfarazi, et al.
Community Genetics|February 13, 2004
The frequency of inherited disorders database: prevalence of Huntington diseaseL N Al-Jader, P S Harper, M Krawczak, et al.
Obstetrics and Gynecology|December 1, 1971
George Otto Gey. (1899-1970). The HeLa cell and a reappraisal of its originH W Jones, V A McKusick, P S Harper, et al.
Muscle & Nerve|May 1, 1991
Assessment of locomotor function in young boys with Duchenne muscular dystrophyR A Smith, R G Newcombe, J R Sibert, et al.
Journal of Medical Genetics|December 1, 1986
Molecular deletion analysis in Duchenne muscular dystrophyN S Thomas, P N Ray, R G Worton, et al.
Journal of Medical Genetics|August 1, 1989
A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probesM Upadhyaya, M Sarfarazi, P W Lunt, et al.
Human Molecular Genetics|April 18, 1998
Huntingtin interacts with cystathionine beta-synthaseJ M Boutell, J D Wood, P S Harper, et al.
Human Genetics|April 1, 1987
X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localizationA Clarke, M Sarfarazi, N S Thomas, et al.
Journal of Medical Genetics|December 1, 1982
A clinical and genetic study of Hunter's syndrome. 1. HeterogeneityI D Young, P S Harper, I M Archer, et al.
Lancet (London, England)|September 9, 1989
Problems in genetic prediction for Huntington's diseaseM J Morris, A Tyler, L Lazarou, et al.
Pageof 35