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B T Darras

Showing results (31-40 of 55) with videos related to

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Gene|February 14, 1990
Novel use of a chimpanzee pseudogene for chromosomal mapping of human cytochrome c oxidase subunit IVM I Lomax, M D Welch, B T Darras, et al.
American Journal of Human Genetics|July 1, 1989
Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneityU Francke, B T Darras, J H Hersh, et al.
Human Mutation|June 30, 2000
Identification of a novel truncating mutation (S171X) in the Emerin gene in five members of a Caucasian American family with Emery-Dreifuss muscular dystrophyC C Menache, C A Brown, J H Donnelly, et al.
Neurology|August 5, 2009
Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutationI A Anselm, K J Sweadner, S Gollamudi, et al.
BMC Genetics|November 17, 2001
Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencingR R Bennett, J den Dunnen, K F O'Brien, et al.
American Journal of Human Genetics|November 1, 1988
Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutationsB T Darras, P Blattner, J F Harper, et al.
Neurosurgery|June 1, 1996
Clonal analysis of meningiomasJ K Wu, M MacGillavry, C Kessaris, et al.
Journal of Child Neurology|April 1, 1986
Globoid cell leukodystrophy: cranial computed tomography and evoked potentialsB T Darras, E S Kwan, H E Gilmore, et al.
Neuromuscular Disorders : NMD|June 27, 2006
Atypical presentations of spinal muscular atrophy type III (Kugelberg-Welander disease)P B Kang, K S Krishnamoorthy, R M Jones, et al.
Neurology|March 1, 1986
Familial amyloidosis with cranial neuropathy and corneal lattice dystrophyB T Darras, L S Adelman, J S Mora, et al.
Pageof 6

Showing results (31-40 of 55) with videos related to

Sort By:
Pageof 6
Gene|February 14, 1990
Novel use of a chimpanzee pseudogene for chromosomal mapping of human cytochrome c oxidase subunit IVM I Lomax, M D Welch, B T Darras, et al.
American Journal of Human Genetics|July 1, 1989
Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneityU Francke, B T Darras, J H Hersh, et al.
Human Mutation|June 30, 2000
Identification of a novel truncating mutation (S171X) in the Emerin gene in five members of a Caucasian American family with Emery-Dreifuss muscular dystrophyC C Menache, C A Brown, J H Donnelly, et al.
Neurology|August 5, 2009
Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutationI A Anselm, K J Sweadner, S Gollamudi, et al.
BMC Genetics|November 17, 2001
Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencingR R Bennett, J den Dunnen, K F O'Brien, et al.
American Journal of Human Genetics|November 1, 1988
Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutationsB T Darras, P Blattner, J F Harper, et al.
Neurosurgery|June 1, 1996
Clonal analysis of meningiomasJ K Wu, M MacGillavry, C Kessaris, et al.
Journal of Child Neurology|April 1, 1986
Globoid cell leukodystrophy: cranial computed tomography and evoked potentialsB T Darras, E S Kwan, H E Gilmore, et al.
Neuromuscular Disorders : NMD|June 27, 2006
Atypical presentations of spinal muscular atrophy type III (Kugelberg-Welander disease)P B Kang, K S Krishnamoorthy, R M Jones, et al.
Neurology|March 1, 1986
Familial amyloidosis with cranial neuropathy and corneal lattice dystrophyB T Darras, L S Adelman, J S Mora, et al.
Pageof 6