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G K Brown

Showing results (1-10 of 117) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1992
Pyruvate dehydrogenase E1 alpha deficiencyG K Brown
Australian Paediatric Journal|January 1, 1988
Recombinant DNA techniques in medicineG K Brown
Journal of Inherited Metabolic Disease|May 4, 2005
Congenital brain malformations in mitochondrial diseaseG K Brown
Journal of Abnormal Psychology|May 1, 1990
A causal analysis of chronic pain and depressionG K Brown
Journal of Inherited Metabolic Disease|January 1, 1994
Metabolic disorders of embryogenesisG K Brown
Journal of Inherited Metabolic Disease|June 23, 2000
Glucose transporters: structure, function and consequences of deficiencyG K Brown
Journal of Inherited Metabolic Disease|March 1, 1997
Bottlenecks and beyond: mitochondrial DNA segregation in health and diseaseG K Brown
Archives of Disease in Childhood|August 1, 1995
Investigation of mitochondrial diseaseJ Poulton, G K Brown
Journal of Inherited Metabolic Disease|January 1, 1996
Complementation analysis of systemic cytochrome oxidase deficiency presenting as Leigh syndromeR M Brown, G K Brown
Human Mutation|January 1, 1994
Pyruvate dehydrogenase deficiency in a male caused by a point mutation (F205L) in the E1 alpha subunitH H Dahl, G K Brown
Pageof 12

Showing results (1-10 of 117) with videos related to

Sort By:
Pageof 12
Journal of Inherited Metabolic Disease|January 1, 1992
Pyruvate dehydrogenase E1 alpha deficiencyG K Brown
Australian Paediatric Journal|January 1, 1988
Recombinant DNA techniques in medicineG K Brown
Journal of Inherited Metabolic Disease|May 4, 2005
Congenital brain malformations in mitochondrial diseaseG K Brown
Journal of Abnormal Psychology|May 1, 1990
A causal analysis of chronic pain and depressionG K Brown
Journal of Inherited Metabolic Disease|January 1, 1994
Metabolic disorders of embryogenesisG K Brown
Journal of Inherited Metabolic Disease|June 23, 2000
Glucose transporters: structure, function and consequences of deficiencyG K Brown
Journal of Inherited Metabolic Disease|March 1, 1997
Bottlenecks and beyond: mitochondrial DNA segregation in health and diseaseG K Brown
Archives of Disease in Childhood|August 1, 1995
Investigation of mitochondrial diseaseJ Poulton, G K Brown
Journal of Inherited Metabolic Disease|January 1, 1996
Complementation analysis of systemic cytochrome oxidase deficiency presenting as Leigh syndromeR M Brown, G K Brown
Human Mutation|January 1, 1994
Pyruvate dehydrogenase deficiency in a male caused by a point mutation (F205L) in the E1 alpha subunitH H Dahl, G K Brown
Pageof 12