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J R Gilbert

Showing results (81-90 of 120) with videos related to

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Lancet (London, England)|November 14, 1987
Inherited deletion at Duchenne dystrophy locus in normal maleJ Koh, R J Bartlett, M A Pericak-Vance, et al.
Neurology|January 19, 2007
Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4K L Deak, R J L F Lemmers, J M Stajich, et al.
Neurobiology of Disease|June 1, 1996
Human apolipoprotein E2, E3, and E4 isoform-specific transgenic mice: human-like pattern of glial and neuronal immunoreactivity in central nervous system not observed in wild-type miceP T Xu, D Schmechel, T Rothrock-Christian, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 10, 2006
Lack of association between UBQLN1 and Alzheimer diseaseM A Slifer, E R Martin, P G Bronson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 10, 2005
Ordered-subset analysis of savant skills in autism for 15q11-q13D Q Ma, J Jaworski, M M Menold, et al.
Genes, Brain, and Behavior|August 14, 2009
Examination of tetrahydrobiopterin pathway genes in autismN C Schnetz-Boutaud, B M Anderson, K D Brown, et al.
Neurology|February 1, 1987
Prenatal detection of an inherited Duchenne muscular dystrophy deletion alleleR J Bartlett, M A Pericak-Vance, J T Lanman, et al.
Australian Paediatric Journal|January 1, 1988
Myotonic dystrophy: update on progress to define the geneA D Roses, M A Pericak-Vance, R J Bartlett, et al.
Ophthalmology|August 12, 1999
Analysis of the Stargardt disease gene (ABCR) in age-related macular degenerationM A De La Paz, V K Guy, S Abou-Donia, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 10, 2009
Association and gene-gene interaction of SLC6A4 and ITGB3 in autismD Q Ma, R Rabionet, I Konidari, et al.
Pageof 12

Showing results (81-90 of 120) with videos related to

Sort By:
Pageof 12
Lancet (London, England)|November 14, 1987
Inherited deletion at Duchenne dystrophy locus in normal maleJ Koh, R J Bartlett, M A Pericak-Vance, et al.
Neurology|January 19, 2007
Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4K L Deak, R J L F Lemmers, J M Stajich, et al.
Neurobiology of Disease|June 1, 1996
Human apolipoprotein E2, E3, and E4 isoform-specific transgenic mice: human-like pattern of glial and neuronal immunoreactivity in central nervous system not observed in wild-type miceP T Xu, D Schmechel, T Rothrock-Christian, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 10, 2006
Lack of association between UBQLN1 and Alzheimer diseaseM A Slifer, E R Martin, P G Bronson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 10, 2005
Ordered-subset analysis of savant skills in autism for 15q11-q13D Q Ma, J Jaworski, M M Menold, et al.
Genes, Brain, and Behavior|August 14, 2009
Examination of tetrahydrobiopterin pathway genes in autismN C Schnetz-Boutaud, B M Anderson, K D Brown, et al.
Neurology|February 1, 1987
Prenatal detection of an inherited Duchenne muscular dystrophy deletion alleleR J Bartlett, M A Pericak-Vance, J T Lanman, et al.
Australian Paediatric Journal|January 1, 1988
Myotonic dystrophy: update on progress to define the geneA D Roses, M A Pericak-Vance, R J Bartlett, et al.
Ophthalmology|August 12, 1999
Analysis of the Stargardt disease gene (ABCR) in age-related macular degenerationM A De La Paz, V K Guy, S Abou-Donia, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 10, 2009
Association and gene-gene interaction of SLC6A4 and ITGB3 in autismD Q Ma, R Rabionet, I Konidari, et al.
Pageof 12