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J L Mandel

Showing results (231-240 of 257) with videos related to

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Human Genetics|October 1, 1987
Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)S Malcolm, G de Saint Basile, B Arveiler, et al.
Biochemical and Biophysical Research Communications|January 13, 1998
Another link between phospholipid transmembrane migration and ABC transporter gene family, inferred from a rare inherited disorder of phosphatidylserine externalizationF Toti, V Schindler, J F Riou, et al.
Human Genetics|January 1, 1986
Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosomeI Oberlé, G Camerino, C Kloepfer, et al.
Lancet (London, England)|March 23, 1985
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPsE Bakker, M H Hofker, N Goor, et al.
Genomics|January 1, 1989
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked markerR Fujita, Y Agid, P Trouillas, et al.
Genomics|January 1, 1991
Genetic mapping of new RFLPs at Xq27-q28G K Suthers, I Oberlé, J Nancarrow, et al.
Neurogenetics|March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1C Ben Hamida, L Cavalier, S Belal, et al.
Human Molecular Genetics|January 1, 1996
Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb regionL J Hu, J Laporte, W Kress, et al.
Human Mutation|May 2, 2000
MTM1 mutations in X-linked myotubular myopathyJ Laporte, V Biancalana, S M Tanner, et al.
Neuron|August 1, 1997
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3H L Paulson, M K Perez, Y Trottier, et al.
Pageof 26

Showing results (231-240 of 257) with videos related to

Sort By:
Pageof 26
Human Genetics|October 1, 1987
Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)S Malcolm, G de Saint Basile, B Arveiler, et al.
Biochemical and Biophysical Research Communications|January 13, 1998
Another link between phospholipid transmembrane migration and ABC transporter gene family, inferred from a rare inherited disorder of phosphatidylserine externalizationF Toti, V Schindler, J F Riou, et al.
Human Genetics|January 1, 1986
Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosomeI Oberlé, G Camerino, C Kloepfer, et al.
Lancet (London, England)|March 23, 1985
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPsE Bakker, M H Hofker, N Goor, et al.
Genomics|January 1, 1989
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked markerR Fujita, Y Agid, P Trouillas, et al.
Genomics|January 1, 1991
Genetic mapping of new RFLPs at Xq27-q28G K Suthers, I Oberlé, J Nancarrow, et al.
Neurogenetics|March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1C Ben Hamida, L Cavalier, S Belal, et al.
Human Molecular Genetics|January 1, 1996
Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb regionL J Hu, J Laporte, W Kress, et al.
Human Mutation|May 2, 2000
MTM1 mutations in X-linked myotubular myopathyJ Laporte, V Biancalana, S M Tanner, et al.
Neuron|August 1, 1997
Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3H L Paulson, M K Perez, Y Trottier, et al.
Pageof 26