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M R Hayden

Showing results (141-150 of 342) with videos related to

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The Journal of Investigative Dermatology|March 1, 1987
Arrested epidermal morphogenesis in three newborn infants with a fatal genetic disorder (restrictive dermopathy)K A Holbrook, B A Dale, D R Witt, et al.
Human Mutation|January 1, 1992
Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosisO Riess, B Weber, A Noeremolle, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 1, 1995
Mapping of the gonadotropin-releasing hormone (GnRH) receptor gene to human chromosome 4q21.2 by fluorescence in situ hybridizationP C Leung, J Squire, C Peng, et al.
The Journal of Clinical Investigation|May 1, 1993
Gene-environment interaction in the conversion of a mild-to-severe phenotype in a patient homozygous for a Ser172-->Cys mutation in the lipoprotein lipase geneY Ma, M S Liu, D Ginzinger, et al.
American Journal of Human Genetics|May 1, 1987
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemiasM R Hayden, H Kirk, C Clark, et al.
Neurology|September 1, 1987
The combined use of positron emission tomography and DNA polymorphisms for preclinical detection of Huntington's diseaseM R Hayden, J Hewitt, A J Stoessl, et al.
American Journal of Human Genetics|February 1, 1992
Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease regionB Weber, A Hedrick, S Andrew, et al.
Clinical Genetics|May 20, 1999
Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standardO Bruland, E W Almqvist, Y P Goldberg, et al.
American Journal of Human Genetics|August 1, 1995
Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomesB Kremer, E Almqvist, J Theilmann, et al.
Journal of Neurochemistry|April 27, 1999
Subtype-specific enhancement of NMDA receptor currents by mutant huntingtinN Chen, T Luo, C Wellington, et al.
Pageof 35

Showing results (141-150 of 342) with videos related to

Sort By:
Pageof 35
The Journal of Investigative Dermatology|March 1, 1987
Arrested epidermal morphogenesis in three newborn infants with a fatal genetic disorder (restrictive dermopathy)K A Holbrook, B A Dale, D R Witt, et al.
Human Mutation|January 1, 1992
Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosisO Riess, B Weber, A Noeremolle, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 1, 1995
Mapping of the gonadotropin-releasing hormone (GnRH) receptor gene to human chromosome 4q21.2 by fluorescence in situ hybridizationP C Leung, J Squire, C Peng, et al.
The Journal of Clinical Investigation|May 1, 1993
Gene-environment interaction in the conversion of a mild-to-severe phenotype in a patient homozygous for a Ser172-->Cys mutation in the lipoprotein lipase geneY Ma, M S Liu, D Ginzinger, et al.
American Journal of Human Genetics|May 1, 1987
DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemiasM R Hayden, H Kirk, C Clark, et al.
Neurology|September 1, 1987
The combined use of positron emission tomography and DNA polymorphisms for preclinical detection of Huntington's diseaseM R Hayden, J Hewitt, A J Stoessl, et al.
American Journal of Human Genetics|February 1, 1992
Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease regionB Weber, A Hedrick, S Andrew, et al.
Clinical Genetics|May 20, 1999
Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standardO Bruland, E W Almqvist, Y P Goldberg, et al.
American Journal of Human Genetics|August 1, 1995
Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomesB Kremer, E Almqvist, J Theilmann, et al.
Journal of Neurochemistry|April 27, 1999
Subtype-specific enhancement of NMDA receptor currents by mutant huntingtinN Chen, T Luo, C Wellington, et al.
Pageof 35