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J Zschocke

Showing results (1-10 of 86) with videos related to

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Journal of Inherited Metabolic Disease|July 15, 2000
Biochemical and molecular studies in mild flavin monooxygenase 3 deficiencyJ Zschocke, E Mayatepek
Human Genetics|July 8, 1999
Phenylketonuria mutations in GermanyJ Zschocke, G F Hoffmann
Lancet (London, England)|May 16, 2003
Homozygous familial hypercholesterolaemia in identical twinsJ Zschocke, J R Schaefer
Journal of Inherited Metabolic Disease|January 1, 1995
Transient neonatal hyperphenylalaninaemia is not related to mutations at the phenylalanine hydroxylase geneJ Zschocke, D J Carson
Molecular and Cellular Probes|December 1, 1995
A fluorescent multiplex ARMS method for rapid mutation analysisJ Zschocke, C A Graham
Methods in Molecular Biology (Clifton, N.J.)|March 27, 2001
Cycle sequencing of polymerase chain reaction-amplified genomic DNA with dye-labeled universal primersJ Zschocke, G F Hoffmann
European Journal of Pediatrics|October 24, 2000
PAH gene mutation analysis in clinical practice--comments on mutation analysis anticipates dietary requirements in phenylketonuriaJ Zschocke, G F Hoffmann
Journal of Inherited Metabolic Disease|July 17, 1999
Glutaric aciduria type I: from clinical, biochemical and molecular diversity to successful therapyG F Hoffmann, J Zschocke
Journal of Inherited Metabolic Disease|October 27, 2004
Isobutyryl-CoA dehydrogenase deficiency: isobutyrylglycinuria and ACAD8 gene mutations in two infantsJ O Sass, S Sander, J Zschocke
Journal of Inherited Metabolic Disease|December 22, 1999
Urinary excretion of Krebs cycle metabolites in a 13-year-old girlJ Zschocke, G Koch, G F Hoffmann
Pageof 9

Showing results (1-10 of 86) with videos related to

Sort By:
Pageof 9
Journal of Inherited Metabolic Disease|July 15, 2000
Biochemical and molecular studies in mild flavin monooxygenase 3 deficiencyJ Zschocke, E Mayatepek
Human Genetics|July 8, 1999
Phenylketonuria mutations in GermanyJ Zschocke, G F Hoffmann
Lancet (London, England)|May 16, 2003
Homozygous familial hypercholesterolaemia in identical twinsJ Zschocke, J R Schaefer
Journal of Inherited Metabolic Disease|January 1, 1995
Transient neonatal hyperphenylalaninaemia is not related to mutations at the phenylalanine hydroxylase geneJ Zschocke, D J Carson
Molecular and Cellular Probes|December 1, 1995
A fluorescent multiplex ARMS method for rapid mutation analysisJ Zschocke, C A Graham
Methods in Molecular Biology (Clifton, N.J.)|March 27, 2001
Cycle sequencing of polymerase chain reaction-amplified genomic DNA with dye-labeled universal primersJ Zschocke, G F Hoffmann
European Journal of Pediatrics|October 24, 2000
PAH gene mutation analysis in clinical practice--comments on mutation analysis anticipates dietary requirements in phenylketonuriaJ Zschocke, G F Hoffmann
Journal of Inherited Metabolic Disease|July 17, 1999
Glutaric aciduria type I: from clinical, biochemical and molecular diversity to successful therapyG F Hoffmann, J Zschocke
Journal of Inherited Metabolic Disease|October 27, 2004
Isobutyryl-CoA dehydrogenase deficiency: isobutyrylglycinuria and ACAD8 gene mutations in two infantsJ O Sass, S Sander, J Zschocke
Journal of Inherited Metabolic Disease|December 22, 1999
Urinary excretion of Krebs cycle metabolites in a 13-year-old girlJ Zschocke, G Koch, G F Hoffmann
Pageof 9