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S Malcolm

Showing results (61-70 of 271) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|September 28, 1973
A gas chromatographic assay for medazepam and its major metabolites in plasmaE S Baird, D M Hailey, S Malcolm
Human Genetics|October 1, 1986
Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)K D MacDermot, R M Winter, S Malcolm
Nature|October 31, 1991
Isodisomy in BWS chromosomesA O Wilkie, S Malcolm, M E Pembrey
Journal of Inherited Metabolic Disease|January 1, 1993
The molecular detection of the pseudodeficiency allele for arylsulphatase A in patients with neurological symptoms and low arylsulphatase A activityS Goldenfum, S Malcolm, E Young, et al.
Journal of Medical Genetics|April 1, 1989
Guidelines for DNA banking. Report of the Clinical Genetics Society working party on DNA bankingJ R Yates, S Malcolm, A P Read
American Journal of Human Genetics|June 23, 1998
Pelizaeus-Merzbacher disease: identification of Xq22 proteolipid-protein duplications and characterization of breakpoints by interphase FISHK Woodward, E Kendall, D Vetrie, et al.
Annals of Human Genetics|February 20, 2002
Nonsyndromic cleft lip and palate: complex genetics and environmental effectsN J Prescott, R M Winter, S Malcolm
The New Zealand Medical Journal|December 22, 1999
Something in the water? A health impact assessment of disinfection by-products in New ZealandM S Malcolm, P Weinstein, A J Woodward
Human Molecular Genetics|July 1, 1993
Mutation analysis in patients with the typical form of Anderson-Fabry diseaseJ P Davies, B G Winchester, S Malcolm
Nucleic Acids Research|April 25, 1989
A new polymorphism for the dystrophin intragenic probe P20 [DXS269] using BstX1M E Robertson, M C Wapenaar, S Malcolm
Pageof 28

Showing results (61-70 of 271) with videos related to

Sort By:
Pageof 28
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 28, 1973
A gas chromatographic assay for medazepam and its major metabolites in plasmaE S Baird, D M Hailey, S Malcolm
Human Genetics|October 1, 1986
Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)K D MacDermot, R M Winter, S Malcolm
Nature|October 31, 1991
Isodisomy in BWS chromosomesA O Wilkie, S Malcolm, M E Pembrey
Journal of Inherited Metabolic Disease|January 1, 1993
The molecular detection of the pseudodeficiency allele for arylsulphatase A in patients with neurological symptoms and low arylsulphatase A activityS Goldenfum, S Malcolm, E Young, et al.
Journal of Medical Genetics|April 1, 1989
Guidelines for DNA banking. Report of the Clinical Genetics Society working party on DNA bankingJ R Yates, S Malcolm, A P Read
American Journal of Human Genetics|June 23, 1998
Pelizaeus-Merzbacher disease: identification of Xq22 proteolipid-protein duplications and characterization of breakpoints by interphase FISHK Woodward, E Kendall, D Vetrie, et al.
Annals of Human Genetics|February 20, 2002
Nonsyndromic cleft lip and palate: complex genetics and environmental effectsN J Prescott, R M Winter, S Malcolm
The New Zealand Medical Journal|December 22, 1999
Something in the water? A health impact assessment of disinfection by-products in New ZealandM S Malcolm, P Weinstein, A J Woodward
Human Molecular Genetics|July 1, 1993
Mutation analysis in patients with the typical form of Anderson-Fabry diseaseJ P Davies, B G Winchester, S Malcolm
Nucleic Acids Research|April 25, 1989
A new polymorphism for the dystrophin intragenic probe P20 [DXS269] using BstX1M E Robertson, M C Wapenaar, S Malcolm
Pageof 28