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H Northrup

Showing results (11-20 of 68) with videos related to

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American Journal of Human Genetics|October 9, 2001
Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viabilityK A Volcik, S H Blanton, H Northrup
Journal of Child Neurology|January 9, 1999
Tuberous sclerosis complex consensus conference: revised clinical diagnostic criteriaE S Roach, M R Gomez, H Northrup
Archives of Dermatology|March 1, 1993
Exfoliative erythroderma resulting from inadequate intake of branched-chain amino acids in infants with maple syrup urine diseaseH Northrup, E S Sigman, A A Hebert
Biophysical Journal|January 1, 1986
Simulation of biomolecular diffusion and complex formationS A Allison, S H Northrup, J A McCammon
Science (New York, N.Y.)|July 1, 1988
Brownian dynamics of cytochrome c and cytochrome c peroxidase associationS H Northrup, J O Boles, J C Reynolds
Journal of Medical Genetics|November 1, 1995
Evaluation of candidate genes for familial brachydactylyJ M Mastrobattista, P Dollé, S H Blanton, et al.
American Journal of Medical Genetics|December 30, 1996
Brachmann-de Lange syndrome: autosomal dominant inheritance and male-to-male transmissionR R McKenney, F F Elder, J Garcia, et al.
Nucleic Acids Research|February 25, 1989
Additional polymorphism for D7S8 linked to cystic fibrosis including detection by DNA amplificationH Northrup, C Rosenbloom, W E O'Brien, et al.
Journal of Child Neurology|July 1, 1999
Tuberous Sclerosis Consensus Conference: recommendations for diagnostic evaluation. National Tuberous Sclerosis AssociationE S Roach, F J DiMario, R S Kandt, et al.
Journal of Medical Genetics|January 1, 1993
Variability of expression in tuberous sclerosisH Northrup, J W Wheless, T K Bertin, et al.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|October 9, 2001
Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viabilityK A Volcik, S H Blanton, H Northrup
Journal of Child Neurology|January 9, 1999
Tuberous sclerosis complex consensus conference: revised clinical diagnostic criteriaE S Roach, M R Gomez, H Northrup
Archives of Dermatology|March 1, 1993
Exfoliative erythroderma resulting from inadequate intake of branched-chain amino acids in infants with maple syrup urine diseaseH Northrup, E S Sigman, A A Hebert
Biophysical Journal|January 1, 1986
Simulation of biomolecular diffusion and complex formationS A Allison, S H Northrup, J A McCammon
Science (New York, N.Y.)|July 1, 1988
Brownian dynamics of cytochrome c and cytochrome c peroxidase associationS H Northrup, J O Boles, J C Reynolds
Journal of Medical Genetics|November 1, 1995
Evaluation of candidate genes for familial brachydactylyJ M Mastrobattista, P Dollé, S H Blanton, et al.
American Journal of Medical Genetics|December 30, 1996
Brachmann-de Lange syndrome: autosomal dominant inheritance and male-to-male transmissionR R McKenney, F F Elder, J Garcia, et al.
Nucleic Acids Research|February 25, 1989
Additional polymorphism for D7S8 linked to cystic fibrosis including detection by DNA amplificationH Northrup, C Rosenbloom, W E O'Brien, et al.
Journal of Child Neurology|July 1, 1999
Tuberous Sclerosis Consensus Conference: recommendations for diagnostic evaluation. National Tuberous Sclerosis AssociationE S Roach, F J DiMario, R S Kandt, et al.
Journal of Medical Genetics|January 1, 1993
Variability of expression in tuberous sclerosisH Northrup, J W Wheless, T K Bertin, et al.
Pageof 7