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C Speer

Showing results (81-90 of 158) with videos related to

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Genomics|October 1, 1993
Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 regionE W Jabs, X Li, M Lovett, et al.
Clinical Genetics|April 16, 2003
Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defectsE Rampersaud, E C Melvin, D Siegel, et al.
Neurogenetics|March 25, 2000
Further exclusion of FSHD1B from the telomeric region of 10qM C Speer, M A Pericak-Vance, J M Stajich, et al.
American Journal of Medical Genetics|August 1, 1994
Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningoceleS Chatkupt, M C Speer, Y Ding, et al.
Neurogenetics|December 17, 2002
Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432Marcy C Speer, Felicia Lennon Graham, Erin Bonner, et al.
Journal of Neurosurgery. Pediatrics|April 3, 2012
Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformationsChristina A Markunas, R Shane Tubbs, Roham Moftakhar, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|February 12, 2008
The brain-derived neurotrophic factor VAL66MET polymorphism and cerebral white matter hyperintensities in late-life depressionWarren D Taylor, Stephan Züchner, Douglas R McQuoid, et al.
Clinical Genetics|October 12, 1999
Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative GroupM C Speer, J Nye, D McLone, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|June 26, 2007
Association of AGTR1 with 18-month treatment outcome in late-life depressionDouglas G Kondo, Marcy C Speer, K Ranga Krishnan, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!R S Kandt, M A Pericak-Vance, W Y Hung, et al.
Pageof 16

Showing results (81-90 of 158) with videos related to

Sort By:
Pageof 16
Genomics|October 1, 1993
Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 regionE W Jabs, X Li, M Lovett, et al.
Clinical Genetics|April 16, 2003
Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defectsE Rampersaud, E C Melvin, D Siegel, et al.
Neurogenetics|March 25, 2000
Further exclusion of FSHD1B from the telomeric region of 10qM C Speer, M A Pericak-Vance, J M Stajich, et al.
American Journal of Medical Genetics|August 1, 1994
Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningoceleS Chatkupt, M C Speer, Y Ding, et al.
Neurogenetics|December 17, 2002
Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432Marcy C Speer, Felicia Lennon Graham, Erin Bonner, et al.
Journal of Neurosurgery. Pediatrics|April 3, 2012
Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformationsChristina A Markunas, R Shane Tubbs, Roham Moftakhar, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|February 12, 2008
The brain-derived neurotrophic factor VAL66MET polymorphism and cerebral white matter hyperintensities in late-life depressionWarren D Taylor, Stephan Züchner, Douglas R McQuoid, et al.
Clinical Genetics|October 12, 1999
Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative GroupM C Speer, J Nye, D McLone, et al.
The American Journal of Geriatric Psychiatry : Official Journal of the American Association for Geriatric Psychiatry|June 26, 2007
Association of AGTR1 with 18-month treatment outcome in late-life depressionDouglas G Kondo, Marcy C Speer, K Ranga Krishnan, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!R S Kandt, M A Pericak-Vance, W Y Hung, et al.
Pageof 16