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American Journal of Human Genetics
|
October 9, 2001
Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viability
K A Volcik, S H Blanton, H Northrup
Journal of Child Neurology
|
January 9, 1999
Tuberous sclerosis complex consensus conference: revised clinical diagnostic criteria
E 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 disease
H Northrup, E S Sigman, A A Hebert
Biophysical Journal
|
January 1, 1986
Simulation of biomolecular diffusion and complex formation
S 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 association
S H Northrup, J O Boles, J C Reynolds
Journal of Medical Genetics
|
November 1, 1995
Evaluation of candidate genes for familial brachydactyly
J 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 transmission
R 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 amplification
H 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 Association
E S Roach, F J DiMario, R S Kandt, et al.
Journal of Medical Genetics
|
January 1, 1993
Variability of expression in tuberous sclerosis
H Northrup, J W Wheless, T K Bertin, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 68) with videos related to
Sort By:
Page
of 7
American Journal of Human Genetics
|
October 9, 2001
Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viability
K A Volcik, S H Blanton, H Northrup
Journal of Child Neurology
|
January 9, 1999
Tuberous sclerosis complex consensus conference: revised clinical diagnostic criteria
E 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 disease
H Northrup, E S Sigman, A A Hebert
Biophysical Journal
|
January 1, 1986
Simulation of biomolecular diffusion and complex formation
S 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 association
S H Northrup, J O Boles, J C Reynolds
Journal of Medical Genetics
|
November 1, 1995
Evaluation of candidate genes for familial brachydactyly
J 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 transmission
R 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 amplification
H 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 Association
E S Roach, F J DiMario, R S Kandt, et al.
Journal of Medical Genetics
|
January 1, 1993
Variability of expression in tuberous sclerosis
H Northrup, J W Wheless, T K Bertin, et al.
Page
of 7