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S Malcolm

Showing results (221-230 of 271) with videos related to

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Canadian Journal of Microbiology|October 1, 1983
Collaborative study of the MPN, Anderson-Baird-Parker direct plating, and hydrophobic grid-membrane filter methods for the enumeration of Escherichia coli biotype I in foodsA N Sharpe, M K Rayman, D M Burgener, et al.
British Journal of Audiology|April 1, 1992
Clinical and genetic heterogeneity in X-linked deafnessW Reardon, H R Middleton-Price, S Malcolm, et al.
Nature Genetics|February 1, 1995
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypesP Rutland, L J Pulleyn, W Reardon, et al.
Journal of Dairy Science|March 4, 2026
The effects of pasteurization on caseinate-based edible film solutionsM J McAnulty, B M Plumier, G K Guron, et al.
British Journal of Pharmacology|September 28, 1999
Functional characterization of agonists at recombinant human 5-HT2A, 5-HT2B and 5-HT2C receptors in CHO-K1 cellsR H Porter, K R Benwell, H Lamb, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 15C Joyce, L Fanning, S Malcolm, et al.
Journal of Medical Genetics|December 1, 1994
Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal familiesM Bitner-Glindzicz, Y de Kok, D Summers, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
Nature Genetics|November 1, 1994
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndromeM Muenke, U Schell, A Hehr, et al.
The Science of the Total Environment|July 4, 2014
Coastal Zone Ecosystem Services: from science to values and decision making; a case studyT Luisetti, R K Turner, T Jickells, et al.
Pageof 28

Showing results (221-230 of 271) with videos related to

Sort By:
Pageof 28
Canadian Journal of Microbiology|October 1, 1983
Collaborative study of the MPN, Anderson-Baird-Parker direct plating, and hydrophobic grid-membrane filter methods for the enumeration of Escherichia coli biotype I in foodsA N Sharpe, M K Rayman, D M Burgener, et al.
British Journal of Audiology|April 1, 1992
Clinical and genetic heterogeneity in X-linked deafnessW Reardon, H R Middleton-Price, S Malcolm, et al.
Nature Genetics|February 1, 1995
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypesP Rutland, L J Pulleyn, W Reardon, et al.
Journal of Dairy Science|March 4, 2026
The effects of pasteurization on caseinate-based edible film solutionsM J McAnulty, B M Plumier, G K Guron, et al.
British Journal of Pharmacology|September 28, 1999
Functional characterization of agonists at recombinant human 5-HT2A, 5-HT2B and 5-HT2C receptors in CHO-K1 cellsR H Porter, K R Benwell, H Lamb, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
The EUROGEM map of human chromosome 15C Joyce, L Fanning, S Malcolm, et al.
Journal of Medical Genetics|December 1, 1994
Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal familiesM Bitner-Glindzicz, Y de Kok, D Summers, et al.
Clinical Genetics|April 19, 2003
The contribution of USH1C mutations to syndromic and non-syndromic deafness in the UKD C Blaydon, R F Mueller, T P Hutchin, et al.
Nature Genetics|November 1, 1994
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndromeM Muenke, U Schell, A Hehr, et al.
The Science of the Total Environment|July 4, 2014
Coastal Zone Ecosystem Services: from science to values and decision making; a case studyT Luisetti, R K Turner, T Jickells, et al.
Pageof 28