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S Malcolm

Showing results (201-210 of 271) with videos related to

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Pharmacology, Biochemistry, and Behavior|August 18, 2001
Modulation of 5-HT(2A) receptor-mediated head-twitch behaviour in the rat by 5-HT(2C) receptor agonistsS P Vickers, N Easton, C S Malcolm, et al.
American Journal of Human Genetics|September 1, 1993
Nondisjunction of chromosome 15: origin and recombinationW P Robinson, F Bernasconi, A Mutirangura, et al.
Human Genetics|March 1, 1987
Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletionS V Hodgson, M E Robertson, C N Fear, et al.
Lancet (London, England)|March 23, 1991
Uniparental paternal disomy in Angelman's syndromeS Malcolm, J Clayton-Smith, M Nichols, et al.
Nature|June 22, 1978
Isolation and partial sequence of recombinant plasmids containing human alpha-, beta- and gamma-globin cDNA fragmentsP Little, P Curtis, C Coutelle, et al.
Human Genetics|March 1, 1993
Physical mapping identifies DXS265 as a useful genetic marker for carrier detection and prenatal diagnosis of X-linked agammaglobulinemiaR Lovering, A K Sweatman, M A O'Reilly, et al.
Brain : a Journal of Neurology|January 1, 1997
Hereditary demyelinating neuropathy of infancy. A genetically complex syndromeJ Tyson, D Ellis, U Fairbrother, et al.
Human Genetics|July 1, 1993
Isolation and mapping of discrete DXS101 loci in Xq22 near the X-linked agammaglobulinaemia gene locusM A O'Reilly, A K Sweatman, L D Bradley, et al.
Gene|January 1, 1985
Polyadenylation of a human mitochondrial ribosomal RNA transcript detected by molecular cloningS J Baserga, A J Linnenbach, S Malcolm, et al.
American Journal of Medical Genetics|December 1, 1992
Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome: a consequence of twinningB Winchester, E Young, S Geddes, et al.
Pageof 28

Showing results (201-210 of 271) with videos related to

Sort By:
Pageof 28
Pharmacology, Biochemistry, and Behavior|August 18, 2001
Modulation of 5-HT(2A) receptor-mediated head-twitch behaviour in the rat by 5-HT(2C) receptor agonistsS P Vickers, N Easton, C S Malcolm, et al.
American Journal of Human Genetics|September 1, 1993
Nondisjunction of chromosome 15: origin and recombinationW P Robinson, F Bernasconi, A Mutirangura, et al.
Human Genetics|March 1, 1987
Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletionS V Hodgson, M E Robertson, C N Fear, et al.
Lancet (London, England)|March 23, 1991
Uniparental paternal disomy in Angelman's syndromeS Malcolm, J Clayton-Smith, M Nichols, et al.
Nature|June 22, 1978
Isolation and partial sequence of recombinant plasmids containing human alpha-, beta- and gamma-globin cDNA fragmentsP Little, P Curtis, C Coutelle, et al.
Human Genetics|March 1, 1993
Physical mapping identifies DXS265 as a useful genetic marker for carrier detection and prenatal diagnosis of X-linked agammaglobulinemiaR Lovering, A K Sweatman, M A O'Reilly, et al.
Brain : a Journal of Neurology|January 1, 1997
Hereditary demyelinating neuropathy of infancy. A genetically complex syndromeJ Tyson, D Ellis, U Fairbrother, et al.
Human Genetics|July 1, 1993
Isolation and mapping of discrete DXS101 loci in Xq22 near the X-linked agammaglobulinaemia gene locusM A O'Reilly, A K Sweatman, L D Bradley, et al.
Gene|January 1, 1985
Polyadenylation of a human mitochondrial ribosomal RNA transcript detected by molecular cloningS J Baserga, A J Linnenbach, S Malcolm, et al.
American Journal of Medical Genetics|December 1, 1992
Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome: a consequence of twinningB Winchester, E Young, S Geddes, et al.
Pageof 28