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S M Forrest

Showing results (11-20 of 48) with videos related to

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Human Genetics|September 1, 1992
CpG hotspot causes second mutation in codon 408 of the phenylalanine hydroxylase geneS J Ramus, S M Forrest, J A Saleeba, et al.
Neurogenetics|March 25, 2000
Friedreich's ataxia presenting as adult-onset spastic paraparesisP C Gates, D Paris, S M Forrest, et al.
Archives of Neurology|January 29, 1999
Spinocerebellar ataxia type 2: clinical features of a pedigree displaying prominent frontal-executive dysfunctionE Storey, S M Forrest, J H Shaw, et al.
Human Genetics|May 1, 1991
Polymorphisms in the human X-linked pyruvate dehydrogenase E1 alpha geneH H Dahl, W M Hutchison, Z Guo, et al.
Human Genetics|October 30, 1999
G130V, a common FRDA point mutation, appears to have arisen from a common founderM B Delatycki, M Knight, M Koenig, et al.
Pharmacogenetics|March 27, 2001
A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuriaS M Forrest, M Knight, B R Akerman, et al.
Genomics|September 1, 1991
Simultaneous screening for beta-thalassemia mutations by chemical cleavage of mismatchI Dianzani, C Camaschella, G Saglio, et al.
American Journal of Human Genetics|July 1, 1991
Mutation detection in phenylketonuria by using chemical cleavage of mismatch: importance of using probes from both normal and patient samplesS M Forrest, H H Dahl, D W Howells, et al.
American Journal of Human Genetics|March 1, 1991
Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutationI Dianzani, S M Forrest, C Camaschella, et al.
Journal of Medical Genetics|May 1, 1993
Comparison of genotype and intellectual phenotype in untreated PKU patientsS J Ramus, S M Forrest, D B Pitt, et al.
Pageof 5

Showing results (11-20 of 48) with videos related to

Sort By:
Pageof 5
Human Genetics|September 1, 1992
CpG hotspot causes second mutation in codon 408 of the phenylalanine hydroxylase geneS J Ramus, S M Forrest, J A Saleeba, et al.
Neurogenetics|March 25, 2000
Friedreich's ataxia presenting as adult-onset spastic paraparesisP C Gates, D Paris, S M Forrest, et al.
Archives of Neurology|January 29, 1999
Spinocerebellar ataxia type 2: clinical features of a pedigree displaying prominent frontal-executive dysfunctionE Storey, S M Forrest, J H Shaw, et al.
Human Genetics|May 1, 1991
Polymorphisms in the human X-linked pyruvate dehydrogenase E1 alpha geneH H Dahl, W M Hutchison, Z Guo, et al.
Human Genetics|October 30, 1999
G130V, a common FRDA point mutation, appears to have arisen from a common founderM B Delatycki, M Knight, M Koenig, et al.
Pharmacogenetics|March 27, 2001
A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuriaS M Forrest, M Knight, B R Akerman, et al.
Genomics|September 1, 1991
Simultaneous screening for beta-thalassemia mutations by chemical cleavage of mismatchI Dianzani, C Camaschella, G Saglio, et al.
American Journal of Human Genetics|July 1, 1991
Mutation detection in phenylketonuria by using chemical cleavage of mismatch: importance of using probes from both normal and patient samplesS M Forrest, H H Dahl, D W Howells, et al.
American Journal of Human Genetics|March 1, 1991
Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutationI Dianzani, S M Forrest, C Camaschella, et al.
Journal of Medical Genetics|May 1, 1993
Comparison of genotype and intellectual phenotype in untreated PKU patientsS J Ramus, S M Forrest, D B Pitt, et al.
Pageof 5