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S M Forrest

Showing results (1-10 of 48) with videos related to

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Laterality|October 30, 2004
Genes for left-handedness: how to search for the needle in the haystack?T Van Agtmael, S M Forrest, R Williamson
Journal of Medical Genetics|January 14, 2000
Friedreich ataxia: an overviewM B Delatycki, R Williamson, S M Forrest
Prenatal Diagnosis|February 1, 1992
Use of the chemical cleavage of mismatch method for prenatal diagnosis of alpha-1-antitrypsin deficiencyS M Forrest, P J Dry, R G Cotton
Human Mutation|January 1, 1992
Illegitimate transcription of phenylalanine hydroxylase for detection of mutations in patients with phenylketonuriaS J Ramus, S M Forrest, R G Cotton
Journal of Bacteriology|October 1, 1984
Cloning of the tyrP gene and further characterization of the tyrosine-specific transport system in Escherichia coli K-12P J Wookey, J Pittard, S M Forrest, et al.
Pediatric Research|April 15, 1999
Genotype and intellectual phenotype in untreated phenylketonuria patientsS J Ramus, S M Forrest, D D Pitt, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 21, 2000
Population-specific polymorphisms of the human FMO3 gene: significance for detoxicationJ R Cashman, B R Akerman, S M Forrest, et al.
Journal of Medical Genetics|August 1, 1994
Maternal uniparental disomy of chromosome 13 in a phenotypically normal childH Slater, J H Shaw, G Dawson, et al.
Nucleic Acids Research|December 10, 1987
Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the geneT J Smith, S M Forrest, G S Cross, et al.
American Journal of Human Genetics|August 1, 1990
Insertion of an extra codon for threonine is a cause of dihydropteridine reductase deficiencyD W Howells, S M Forrest, H H Dahl, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Laterality|October 30, 2004
Genes for left-handedness: how to search for the needle in the haystack?T Van Agtmael, S M Forrest, R Williamson
Journal of Medical Genetics|January 14, 2000
Friedreich ataxia: an overviewM B Delatycki, R Williamson, S M Forrest
Prenatal Diagnosis|February 1, 1992
Use of the chemical cleavage of mismatch method for prenatal diagnosis of alpha-1-antitrypsin deficiencyS M Forrest, P J Dry, R G Cotton
Human Mutation|January 1, 1992
Illegitimate transcription of phenylalanine hydroxylase for detection of mutations in patients with phenylketonuriaS J Ramus, S M Forrest, R G Cotton
Journal of Bacteriology|October 1, 1984
Cloning of the tyrP gene and further characterization of the tyrosine-specific transport system in Escherichia coli K-12P J Wookey, J Pittard, S M Forrest, et al.
Pediatric Research|April 15, 1999
Genotype and intellectual phenotype in untreated phenylketonuria patientsS J Ramus, S M Forrest, D D Pitt, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|January 21, 2000
Population-specific polymorphisms of the human FMO3 gene: significance for detoxicationJ R Cashman, B R Akerman, S M Forrest, et al.
Journal of Medical Genetics|August 1, 1994
Maternal uniparental disomy of chromosome 13 in a phenotypically normal childH Slater, J H Shaw, G Dawson, et al.
Nucleic Acids Research|December 10, 1987
Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the geneT J Smith, S M Forrest, G S Cross, et al.
American Journal of Human Genetics|August 1, 1990
Insertion of an extra codon for threonine is a cause of dihydropteridine reductase deficiencyD W Howells, S M Forrest, H H Dahl, et al.
Pageof 5