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N E Simpson

Showing results (51-60 of 91) with videos related to

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Human Heredity|January 1, 1983
HLA haplotype segregation in families of type 1 diabeticsL J Walsh, R M Ehrlich, J A Falk, et al.
Nucleic Acids Research|May 27, 1986
Three RFLPs recognized by an anonymous sequence localized to 21q11.2 [HGM8 D21S72]P J Goodfellow, A M Duncan, N E Simpson, et al.
Canadian Medical Association Journal|September 9, 1978
Hereditary angioneurotic edema and Charcot-Marie-Tooth disease in the same familyP G Fernandez, J H Day, N E Simpson, et al.
Canadian Medical Association Journal|February 15, 1981
Multiple endocrine neoplasia, type II: a combined surgical and genetic approach to treatmentM W Partington, W R Ghent, E V Sears, et al.
Acta Oto-Laryngologica|May 1, 1979
Binocular counterrolling in humans during dynamic rotationS G Diamond, C H Markham, N E Simpson, et al.
Human Genetics|December 18, 1978
Confirmation of regional assignment of nucleoside phosphorylase (NP) on chromosome 14 by gene dosage studiesM Frecker, L Dallaire, S R Young, et al.
Journal of Materials Science. Materials in Medicine|June 2, 2005
Effects of alginate encapsulation on mitochondrial activityJ Oca-Cossio, N E Simpson, Z Han, et al.
Biochemical and Biophysical Research Communications|July 13, 2000
Effects of pH on murine insulinoma betaTC3 cellsN E Simpson, L K Bennett, K K Papas, et al.
American Journal of Medical Genetics|January 1, 1981
Familial cutaneous amyloidosis with systemic manifestations in malesM W Partington, P J Marriott, R S Prentice, et al.
Journal of Neurogenetics|July 1, 1986
Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13J Beckett, J J Holden, N E Simpson, et al.
Pageof 10

Showing results (51-60 of 91) with videos related to

Sort By:
Pageof 10
Human Heredity|January 1, 1983
HLA haplotype segregation in families of type 1 diabeticsL J Walsh, R M Ehrlich, J A Falk, et al.
Nucleic Acids Research|May 27, 1986
Three RFLPs recognized by an anonymous sequence localized to 21q11.2 [HGM8 D21S72]P J Goodfellow, A M Duncan, N E Simpson, et al.
Canadian Medical Association Journal|September 9, 1978
Hereditary angioneurotic edema and Charcot-Marie-Tooth disease in the same familyP G Fernandez, J H Day, N E Simpson, et al.
Canadian Medical Association Journal|February 15, 1981
Multiple endocrine neoplasia, type II: a combined surgical and genetic approach to treatmentM W Partington, W R Ghent, E V Sears, et al.
Acta Oto-Laryngologica|May 1, 1979
Binocular counterrolling in humans during dynamic rotationS G Diamond, C H Markham, N E Simpson, et al.
Human Genetics|December 18, 1978
Confirmation of regional assignment of nucleoside phosphorylase (NP) on chromosome 14 by gene dosage studiesM Frecker, L Dallaire, S R Young, et al.
Journal of Materials Science. Materials in Medicine|June 2, 2005
Effects of alginate encapsulation on mitochondrial activityJ Oca-Cossio, N E Simpson, Z Han, et al.
Biochemical and Biophysical Research Communications|July 13, 2000
Effects of pH on murine insulinoma betaTC3 cellsN E Simpson, L K Bennett, K K Papas, et al.
American Journal of Medical Genetics|January 1, 1981
Familial cutaneous amyloidosis with systemic manifestations in malesM W Partington, P J Marriott, R S Prentice, et al.
Journal of Neurogenetics|July 1, 1986
Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq13J Beckett, J J Holden, N E Simpson, et al.
Pageof 10