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B Kerr

Showing results (311-320 of 350) with videos related to

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Clinical Dysmorphology|November 14, 1997
Macrocephaly with cutis marmorata, haemangioma and syndactyly--a distinctive overgrowth syndromeJ Clayton-Smith, B Kerr, H Brunner, et al.
Nature Genetics|August 10, 2000
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.
Princess Takamatsu Symposia|January 1, 1989
Genetic analysis of colorectal cancerW F Bodmer, S Cottrell, A M Frischauf, et al.
Clinical Genetics|August 21, 2012
MLL2 mosaic mutations and intragenic deletion-duplications in patients with Kabuki syndromeS Banka, E Howard, S Bunstone, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
The adult phenotype in Costello syndromeSusan M White, J M Graham, B Kerr, et al.
Diabetes Technology & Therapeutics|November 24, 2007
Outcomes of a cardiothoracic intensive care web-based online intravenous insulin infusion calculator study at a Medical University HospitalKathie L Hermayer, Diane E Neal, Timothy V Hushion, et al.
Development (Cambridge, England)|September 1, 1991
Sex chimaerism, fertility and sex determination in the mouseC E Patek, J B Kerr, R G Gosden, et al.
Plos One|July 18, 2019
MR susceptibility contrast imaging using a 2D simultaneous multi-slice gradient-echo sequence at 7TWei Bian, Adam B Kerr, Eric Tranvinh, et al.
Cancer|September 11, 2001
Women's attitudes toward preventive strategies for hereditary breast or ovarian carcinoma differ from one country to another: differences among English, French, and Canadian womenC M Julian-Reynier, L J Bouchard, D G Evans, et al.
Journal of Medical Genetics|November 28, 2007
Severe neonatal manifestations of Costello syndromeI F M Lo, C Brewer, N Shannon, et al.
Pageof 35

Showing results (311-320 of 350) with videos related to

Sort By:
Pageof 35
Clinical Dysmorphology|November 14, 1997
Macrocephaly with cutis marmorata, haemangioma and syndactyly--a distinctive overgrowth syndromeJ Clayton-Smith, B Kerr, H Brunner, et al.
Nature Genetics|August 10, 2000
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.
Princess Takamatsu Symposia|January 1, 1989
Genetic analysis of colorectal cancerW F Bodmer, S Cottrell, A M Frischauf, et al.
Clinical Genetics|August 21, 2012
MLL2 mosaic mutations and intragenic deletion-duplications in patients with Kabuki syndromeS Banka, E Howard, S Bunstone, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
The adult phenotype in Costello syndromeSusan M White, J M Graham, B Kerr, et al.
Diabetes Technology & Therapeutics|November 24, 2007
Outcomes of a cardiothoracic intensive care web-based online intravenous insulin infusion calculator study at a Medical University HospitalKathie L Hermayer, Diane E Neal, Timothy V Hushion, et al.
Development (Cambridge, England)|September 1, 1991
Sex chimaerism, fertility and sex determination in the mouseC E Patek, J B Kerr, R G Gosden, et al.
Plos One|July 18, 2019
MR susceptibility contrast imaging using a 2D simultaneous multi-slice gradient-echo sequence at 7TWei Bian, Adam B Kerr, Eric Tranvinh, et al.
Cancer|September 11, 2001
Women's attitudes toward preventive strategies for hereditary breast or ovarian carcinoma differ from one country to another: differences among English, French, and Canadian womenC M Julian-Reynier, L J Bouchard, D G Evans, et al.
Journal of Medical Genetics|November 28, 2007
Severe neonatal manifestations of Costello syndromeI F M Lo, C Brewer, N Shannon, et al.
Pageof 35