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Victoria Murday

Showing results (11-20 of 21) with videos related to

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Cold Spring Harbor Molecular Case Studies|January 5, 2017
Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in <i>NDUFB11</i>Gillian Rea, Tessa Homfray, Jan Till, et al.
Human Molecular Genetics|May 6, 2009
X-linked cataract and Nance-Horan syndrome are allelic disordersMargherita Coccia, Simon P Brooks, Tom R Webb, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 2005
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromesDiana E Benn, Anne-Paule Gimenez-Roqueplo, Jennifer R Reilly, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 27, 2015
Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencingLaurence M Nunn, Luis R Lopes, Petros Syrris, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 19, 2015
Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 StudyMohammad Movahedi, D Timothy Bishop, Finlay Macrae, et al.
The Lancet. Oncology|November 13, 2012
Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trialJohn C Mathers, Mohammad Movahedi, Finlay Macrae, et al.
Nature Genetics|February 19, 2008
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizuresAndrew J Sharp, Heather C Mefford, Kelly Li, et al.
American Journal of Human Genetics|June 7, 2014
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformationsJoe Rainger, Davut Pehlivan, Stefan Johansson, et al.
Lancet (London, England)|November 1, 2011
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trialJohn Burn, Anne-Marie Gerdes, Finlay Macrae, et al.
Journal of Medical Genetics|February 2, 2018
Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes <i>SDHB</i>, <i>SDHC</i> and <i>SDHD</i>Katrina A Andrews, David B Ascher, Douglas Eduardo Valente Pires, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Cold Spring Harbor Molecular Case Studies|January 5, 2017
Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in <i>NDUFB11</i>Gillian Rea, Tessa Homfray, Jan Till, et al.
Human Molecular Genetics|May 6, 2009
X-linked cataract and Nance-Horan syndrome are allelic disordersMargherita Coccia, Simon P Brooks, Tom R Webb, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 2005
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromesDiana E Benn, Anne-Paule Gimenez-Roqueplo, Jennifer R Reilly, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 27, 2015
Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencingLaurence M Nunn, Luis R Lopes, Petros Syrris, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 19, 2015
Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 StudyMohammad Movahedi, D Timothy Bishop, Finlay Macrae, et al.
The Lancet. Oncology|November 13, 2012
Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trialJohn C Mathers, Mohammad Movahedi, Finlay Macrae, et al.
Nature Genetics|February 19, 2008
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizuresAndrew J Sharp, Heather C Mefford, Kelly Li, et al.
American Journal of Human Genetics|June 7, 2014
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformationsJoe Rainger, Davut Pehlivan, Stefan Johansson, et al.
Lancet (London, England)|November 1, 2011
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trialJohn Burn, Anne-Marie Gerdes, Finlay Macrae, et al.
Journal of Medical Genetics|February 2, 2018
Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes <i>SDHB</i>, <i>SDHC</i> and <i>SDHD</i>Katrina A Andrews, David B Ascher, Douglas Eduardo Valente Pires, et al.
Pageof 3