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W G Johnson

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American Journal of Medical Genetics|December 14, 1999
Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in familial spina bifidaW G Johnson, E S Stenroos, S C Heath, et al.
Muscle & Nerve|January 1, 1979
Lipid storage myopathy, ichthyosis, and steatorrheaA Miranda, S DiMauro, A Eastwood, et al.
The Journal of Clinical Investigation|August 1, 1985
Characterization of a new model of GM2-gangliosidosis (Sandhoff's disease) in Korat catsE A Neuwelt, W G Johnson, N K Blank, et al.
The New England Journal of Medicine|July 5, 1973
Replacement therapy for inherited enzyme deficiency. Use of purified ceramidetrihexosidase in Fabry's diseaseR O Brady, J F Tallman, W G Johnson, et al.
JAMA|May 13, 1992
The economic consequences of medical injuries. Implications for a no-fault insurance planW G Johnson, T A Brennan, J P Newhouse, et al.
Obesity Research|May 1, 1997
Dietary and exercise interventions for juvenile obesity: long-term effect of behavioral and public health modelsW G Johnson, L K Hinkle, R E Carr, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 8, 2001
The tau A0 allele in Parkinson's diseaseL I Golbe, A M Lazzarini, J R Spychala, et al.
American Journal of Medical Genetics|July 17, 1995
Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20)A Lazzarini, E S Stenroos, T Lehner, et al.
Annals of Neurology|June 1, 1986
N-acetyl-beta-hexosaminidase beta locus defect and juvenile motor neuron disease: a case studyN R Cashman, J P Antel, L W Hancock, 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.
Pageof 14

Showing results (111-120 of 133) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics|December 14, 1999
Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in familial spina bifidaW G Johnson, E S Stenroos, S C Heath, et al.
Muscle & Nerve|January 1, 1979
Lipid storage myopathy, ichthyosis, and steatorrheaA Miranda, S DiMauro, A Eastwood, et al.
The Journal of Clinical Investigation|August 1, 1985
Characterization of a new model of GM2-gangliosidosis (Sandhoff's disease) in Korat catsE A Neuwelt, W G Johnson, N K Blank, et al.
The New England Journal of Medicine|July 5, 1973
Replacement therapy for inherited enzyme deficiency. Use of purified ceramidetrihexosidase in Fabry's diseaseR O Brady, J F Tallman, W G Johnson, et al.
JAMA|May 13, 1992
The economic consequences of medical injuries. Implications for a no-fault insurance planW G Johnson, T A Brennan, J P Newhouse, et al.
Obesity Research|May 1, 1997
Dietary and exercise interventions for juvenile obesity: long-term effect of behavioral and public health modelsW G Johnson, L K Hinkle, R E Carr, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 8, 2001
The tau A0 allele in Parkinson's diseaseL I Golbe, A M Lazzarini, J R Spychala, et al.
American Journal of Medical Genetics|July 17, 1995
Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20)A Lazzarini, E S Stenroos, T Lehner, et al.
Annals of Neurology|June 1, 1986
N-acetyl-beta-hexosaminidase beta locus defect and juvenile motor neuron disease: a case studyN R Cashman, J P Antel, L W Hancock, 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.
Pageof 14