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H S Scott

Showing results (31-40 of 84) with videos related to

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Genomics|April 18, 1998
Identification and characterization of two putative human arginine methyltransferases (HRMT1L1 and HRMT1L2)H S Scott, S E Antonarakis, M D Lalioti, et al.
Genomics|December 1, 1992
An 86-bp VNTR within IDUA is the basis of the D4S111 polymorphic locusH S Scott, P V Nelson, M E MacDonald, et al.
Human Mutation|January 1, 1994
Mutation analysis of 19 North American mucopolysaccharidosis type I patients: identification of two additional frequent mutationsL A Clarke, P V Nelson, C L Warrington, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|August 31, 1996
Structure and sequence of the human sulphamidase geneL E Karageorgos, X H Guo, L Blanch, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3H S Scott, S E Antonarakis, L Mittaz, et al.
British Journal of Cancer|June 27, 2013
BCR-ABL1 kinase domain mutations may persist at very low levels for many years and lead to subsequent TKI resistanceW T Parker, A L Yeoman, B A Jamison, et al.
Genome Research|June 1, 1997
Cloning of two human homologs of the Drosophila single-minded gene SIM1 on chromosome 6q and SIM2 on 21q within the Down syndrome chromosomal regionR Chrast, H S Scott, H Chen, et al.
American Journal of Human Genetics|November 1, 1993
Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromesH S Scott, T Litjens, P V Nelson, et al.
Nature|April 24, 1997
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsyM D Lalioti, H S Scott, C Buresi, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1991
Human alpha-L-iduronidase: cDNA isolation and expressionH S Scott, D S Anson, A M Orsborn, et al.
Pageof 9

Showing results (31-40 of 84) with videos related to

Sort By:
Pageof 9
Genomics|April 18, 1998
Identification and characterization of two putative human arginine methyltransferases (HRMT1L1 and HRMT1L2)H S Scott, S E Antonarakis, M D Lalioti, et al.
Genomics|December 1, 1992
An 86-bp VNTR within IDUA is the basis of the D4S111 polymorphic locusH S Scott, P V Nelson, M E MacDonald, et al.
Human Mutation|January 1, 1994
Mutation analysis of 19 North American mucopolysaccharidosis type I patients: identification of two additional frequent mutationsL A Clarke, P V Nelson, C L Warrington, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|August 31, 1996
Structure and sequence of the human sulphamidase geneL E Karageorgos, X H Guo, L Blanch, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3H S Scott, S E Antonarakis, L Mittaz, et al.
British Journal of Cancer|June 27, 2013
BCR-ABL1 kinase domain mutations may persist at very low levels for many years and lead to subsequent TKI resistanceW T Parker, A L Yeoman, B A Jamison, et al.
Genome Research|June 1, 1997
Cloning of two human homologs of the Drosophila single-minded gene SIM1 on chromosome 6q and SIM2 on 21q within the Down syndrome chromosomal regionR Chrast, H S Scott, H Chen, et al.
American Journal of Human Genetics|November 1, 1993
Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromesH S Scott, T Litjens, P V Nelson, et al.
Nature|April 24, 1997
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsyM D Lalioti, H S Scott, C Buresi, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1991
Human alpha-L-iduronidase: cDNA isolation and expressionH S Scott, D S Anson, A M Orsborn, et al.
Pageof 9