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S Packman

Showing results (61-70 of 98) with videos related to

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Pediatric Neurology|May 1, 1992
Neurologic complications in galactosemiaT K Koch, K A Schmidt, J E Wagstaff, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1974
Regulated expression of mammalian genes: globin and immunoglobulin as model systemsP Leder, J Ross, J Gielen, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Lipid metabolism in biotin-responsive multiple carboxylase deficiencyM C Gonzalez-Rios, S C Whitney, M L Williams, et al.
Annals of Neurology|November 1, 1980
Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies: a biotin-responsive disorderJ E Sander, N Malamud, M J Cowan, et al.
Clinical Genetics|June 28, 2007
Executive functioning in children and adolescents with phenylketonuriaK H VanZutphen, W Packman, L Sporri, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Prenatal diagnosis of Menkes disease by mutation analysisS Das, S Whitney, J Taylor, et al.
Pediatrics|March 1, 1984
Curious neurologic sequelae in galactosemiaW Lo, S Packman, S Nash, et al.
Clinical Genetics|February 1, 1985
A distinct variant of intermediate maple syrup urine diseaseM C Gonzalez-Rios, D T Chuang, R P Cox, et al.
Pediatric Research|October 6, 1997
Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes diseaseY Murata, H Kodama, T Abe, et al.
Journal of Medical Genetics|April 1, 1984
Location of the retinoblastoma susceptibility gene(s) and the human esterase D locusP Ward, S Packman, W Loughman, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
Pediatric Neurology|May 1, 1992
Neurologic complications in galactosemiaT K Koch, K A Schmidt, J E Wagstaff, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1974
Regulated expression of mammalian genes: globin and immunoglobulin as model systemsP Leder, J Ross, J Gielen, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Lipid metabolism in biotin-responsive multiple carboxylase deficiencyM C Gonzalez-Rios, S C Whitney, M L Williams, et al.
Annals of Neurology|November 1, 1980
Intermittent ataxia and immunodeficiency with multiple carboxylase deficiencies: a biotin-responsive disorderJ E Sander, N Malamud, M J Cowan, et al.
Clinical Genetics|June 28, 2007
Executive functioning in children and adolescents with phenylketonuriaK H VanZutphen, W Packman, L Sporri, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Prenatal diagnosis of Menkes disease by mutation analysisS Das, S Whitney, J Taylor, et al.
Pediatrics|March 1, 1984
Curious neurologic sequelae in galactosemiaW Lo, S Packman, S Nash, et al.
Clinical Genetics|February 1, 1985
A distinct variant of intermediate maple syrup urine diseaseM C Gonzalez-Rios, D T Chuang, R P Cox, et al.
Pediatric Research|October 6, 1997
Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes diseaseY Murata, H Kodama, T Abe, et al.
Journal of Medical Genetics|April 1, 1984
Location of the retinoblastoma susceptibility gene(s) and the human esterase D locusP Ward, S Packman, W Loughman, et al.
Pageof 10