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S Malcolm

Showing results (241-250 of 271) with videos related to

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Journal of Medical Genetics|May 9, 2006
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%A-F Roux, V Faugère, S Le Guédard, et al.
Nature|February 11, 1993
Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgMU Korthäuer, D Graf, H W Mages, et al.
American Journal of Human Genetics|November 1, 1994
Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palateH Feng, R Sassani, S P Bartlett, et al.
Journal of Colloid and Interface Science|May 17, 2011
Comparison of positional surfactant isomers for displacement of rubisco protein from the air-water interfaceLizhong He, Sagheer A Onaizi, Mirjana Dimitrijev-Dwyer, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|August 29, 2009
Cooperative tuneable interactions between a designed peptide biosurfactant and positional isomers of SDOBS at the air-water interfaceLizhong He, Andrew S Malcolm, Mirjana Dimitrijev, et al.
Human Molecular Genetics|February 1, 1993
Genetic linkage analysis identifies new proximal and distal flanking markers for the X-linked agammaglobulinemia gene locus, refining its localization in Xq22R Lovering, H R Middleton-Price, M A O'Reilly, et al.
Clinical Genetics|June 14, 2000
Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15W P Robinson, S L Christian, B D Kuchinka, et al.
Brain : a Journal of Neurology|March 1, 1997
The phenotypic manifestations of chromosome 17p11.2 duplicationP K Thomas, W Marques, M B Davis, et al.
Science (New York, N.Y.)|February 3, 1995
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locusL J Pulleyn, W Reardon, D Wilkes, et al.
Pageof 28

Showing results (241-250 of 271) with videos related to

Sort By:
Pageof 28
Journal of Medical Genetics|May 9, 2006
Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%A-F Roux, V Faugère, S Le Guédard, et al.
Nature|February 11, 1993
Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgMU Korthäuer, D Graf, H W Mages, et al.
American Journal of Human Genetics|November 1, 1994
Evidence, from family studies, for linkage disequilibrium between TGFA and a gene for nonsyndromic cleft lip with or without cleft palateH Feng, R Sassani, S P Bartlett, et al.
Journal of Colloid and Interface Science|May 17, 2011
Comparison of positional surfactant isomers for displacement of rubisco protein from the air-water interfaceLizhong He, Sagheer A Onaizi, Mirjana Dimitrijev-Dwyer, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|August 29, 2009
Cooperative tuneable interactions between a designed peptide biosurfactant and positional isomers of SDOBS at the air-water interfaceLizhong He, Andrew S Malcolm, Mirjana Dimitrijev, et al.
Human Molecular Genetics|February 1, 1993
Genetic linkage analysis identifies new proximal and distal flanking markers for the X-linked agammaglobulinemia gene locus, refining its localization in Xq22R Lovering, H R Middleton-Price, M A O'Reilly, et al.
Clinical Genetics|June 14, 2000
Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15W P Robinson, S L Christian, B D Kuchinka, et al.
Brain : a Journal of Neurology|March 1, 1997
The phenotypic manifestations of chromosome 17p11.2 duplicationP K Thomas, W Marques, M B Davis, et al.
Science (New York, N.Y.)|February 3, 1995
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4Y J de Kok, S M van der Maarel, M Bitner-Glindzicz, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locusL J Pulleyn, W Reardon, D Wilkes, et al.
Pageof 28