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D E Bulman

Showing results (21-30 of 52) with videos related to

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Ophthalmic Genetics|January 5, 2000
Childhood-onset primary open angle glaucoma in a Canadian kindred: clinical and molecular genetic featuresK F Damji, X Song, S K Gupta, et al.
Human Molecular Genetics|May 1, 1993
Genomic organization of exons 22 to 25 of the dystrophin geneK G Bebchuk, D E Bulman, V N D'Souza, et al.
Journal of Medical Genetics|March 19, 2002
A novel locus for brachydactyly type A1 on chromosome 5p13.3-p13.2C M Armour, M E McCready, A Baig, et al.
Genomics|June 1, 1991
Point mutation in the human dystrophin gene: identification through western blot analysisD E Bulman, S B Gangopadhyay, K G Bebchuck, et al.
Muscle & Nerve|May 1, 1990
Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical studyS Carpenter, G Karpati, E Zubrzycka-Gaarn, et al.
American Journal of Medical Genetics|October 1, 1992
Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern of DNA deletionM Vainzof, M R Passos-Bueno, D Rapaport, et al.
American Journal of Human Genetics|February 1, 1991
Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophinD E Bulman, E G Murphy, E E Zubrzycka-Gaarn, et al.
Journal of Medical Genetics|January 15, 2003
Identification of a mutation in the Indian Hedgehog (IHH) gene causing brachydactyly type A1 and evidence for a third locusT J Kirkpatrick, K-S Au, J M Mastrobattista, et al.
Neurology|October 23, 2002
A novel locus for inherited myoclonus-dystonia on 18p11D A Grimes, F Han, A E Lang, et al.
Journal of Neuropathology and Experimental Neurology|March 1, 1990
Age-related conversion of dystrophin-negative to -positive fiber segments of skeletal but not cardiac muscle fibers in heterozygote mdx miceG Karpati, E E Zubrzycka-Gaarn, S Carpenter, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Ophthalmic Genetics|January 5, 2000
Childhood-onset primary open angle glaucoma in a Canadian kindred: clinical and molecular genetic featuresK F Damji, X Song, S K Gupta, et al.
Human Molecular Genetics|May 1, 1993
Genomic organization of exons 22 to 25 of the dystrophin geneK G Bebchuk, D E Bulman, V N D'Souza, et al.
Journal of Medical Genetics|March 19, 2002
A novel locus for brachydactyly type A1 on chromosome 5p13.3-p13.2C M Armour, M E McCready, A Baig, et al.
Genomics|June 1, 1991
Point mutation in the human dystrophin gene: identification through western blot analysisD E Bulman, S B Gangopadhyay, K G Bebchuck, et al.
Muscle & Nerve|May 1, 1990
Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical studyS Carpenter, G Karpati, E Zubrzycka-Gaarn, et al.
American Journal of Medical Genetics|October 1, 1992
Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern of DNA deletionM Vainzof, M R Passos-Bueno, D Rapaport, et al.
American Journal of Human Genetics|February 1, 1991
Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophinD E Bulman, E G Murphy, E E Zubrzycka-Gaarn, et al.
Journal of Medical Genetics|January 15, 2003
Identification of a mutation in the Indian Hedgehog (IHH) gene causing brachydactyly type A1 and evidence for a third locusT J Kirkpatrick, K-S Au, J M Mastrobattista, et al.
Neurology|October 23, 2002
A novel locus for inherited myoclonus-dystonia on 18p11D A Grimes, F Han, A E Lang, et al.
Journal of Neuropathology and Experimental Neurology|March 1, 1990
Age-related conversion of dystrophin-negative to -positive fiber segments of skeletal but not cardiac muscle fibers in heterozygote mdx miceG Karpati, E E Zubrzycka-Gaarn, S Carpenter, et al.
Pageof 6