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E R McCabe

Showing results (31-40 of 160) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
State-of-the-art for DNA technology in newborn screeningE R McCabe, L L McCabe
American Journal of Human Genetics|May 4, 2000
Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamicsK M Dipple, E R McCabe
Molecular and Cellular Biochemistry|September 1, 1984
Subcellular distribution and kinetic properties of soluble and particulate-associated bovine adrenal glycerol kinaseW K Seltzer, E R McCabe
Neonatal Network : NN|February 1, 1988
Newborn screening for inherited metabolic disease: principles and practiceA M Kotzer, E R McCabe
American Journal of Diseases of Children (1960)|November 1, 1978
Recurrent Reye's syndromeM E Pichichero, E R McCabe
Human Mutation|December 19, 2001
Mutations in NR0B1 (DAX1) and NR5A1 (SF1) responsible for adrenal hypoplasia congenitaJ K Phelan, E R McCabe
Gene Expression Patterns : GEP|December 18, 2003
Nr0b1 and its network partners are expressed early in murine embryos prior to steroidogenic axis organogenesisR Clipsham, K Niakan, E R McCabe
The Journal of Pediatrics|May 1, 1995
Dysmorphic features in patients with complex glycerol kinase deficiencyA Scheuerle, F Greenberg, E R McCabe
American Journal of Medical Genetics|May 1, 1989
Weaver syndrome: the changing phenotype in an adultF Greenberg, W Wasiewski, E R McCabe
Biochemical Medicine and Metabolic Biology|October 1, 1994
Hexokinase autophosphorylation: identification of a new dual specificity protein kinaseV Adams, A Schieber, E R McCabe
Pageof 16

Showing results (31-40 of 160) with videos related to

Sort By:
Pageof 16
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
State-of-the-art for DNA technology in newborn screeningE R McCabe, L L McCabe
American Journal of Human Genetics|May 4, 2000
Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamicsK M Dipple, E R McCabe
Molecular and Cellular Biochemistry|September 1, 1984
Subcellular distribution and kinetic properties of soluble and particulate-associated bovine adrenal glycerol kinaseW K Seltzer, E R McCabe
Neonatal Network : NN|February 1, 1988
Newborn screening for inherited metabolic disease: principles and practiceA M Kotzer, E R McCabe
American Journal of Diseases of Children (1960)|November 1, 1978
Recurrent Reye's syndromeM E Pichichero, E R McCabe
Human Mutation|December 19, 2001
Mutations in NR0B1 (DAX1) and NR5A1 (SF1) responsible for adrenal hypoplasia congenitaJ K Phelan, E R McCabe
Gene Expression Patterns : GEP|December 18, 2003
Nr0b1 and its network partners are expressed early in murine embryos prior to steroidogenic axis organogenesisR Clipsham, K Niakan, E R McCabe
The Journal of Pediatrics|May 1, 1995
Dysmorphic features in patients with complex glycerol kinase deficiencyA Scheuerle, F Greenberg, E R McCabe
American Journal of Medical Genetics|May 1, 1989
Weaver syndrome: the changing phenotype in an adultF Greenberg, W Wasiewski, E R McCabe
Biochemical Medicine and Metabolic Biology|October 1, 1994
Hexokinase autophosphorylation: identification of a new dual specificity protein kinaseV Adams, A Schieber, E R McCabe
Pageof 16