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Edward Blair

Showing results (11-20 of 67) with videos related to

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European Journal of Human Genetics : EJHG|February 15, 2018
Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative studyMichael P Mackley, Edward Blair, Michael Parker, et al.
Obstetric Medicine|May 17, 2021
Loeys-Dietz syndrome in pregnancyKatharine E Thomas, Jennifer Hogan, Alex Pitcher, et al.
Microbes and Infection|September 24, 2004
Recombinant respiratory syncytial virus lacking secreted glycoprotein G is attenuated, non-pathogenic but induces protective immunityCaroline F Maher, Tracy Hussell, Edward Blair, et al.
European Journal of Human Genetics : EJHG|June 13, 2019
Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular diseaseJames Buchanan, Edward Blair, Kate L Thomson, et al.
European Heart Journal|March 20, 2010
DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness modelSarah Wordsworth, José Leal, Edward Blair, et al.
Respiration; International Review of Thoracic Diseases|September 26, 2012
The impact of obstructive sleep apnea on aortic disease in Marfan's syndromeMalcolm Kohler, Alex Pitcher, Edward Blair, et al.
Developmental Medicine and Child Neurology|November 22, 2011
Early use of high-dose riboflavin in a case of Brown-Vialetto-Van Laere syndromeGeetha Anand, Nadeem Hasan, Sathiya Jayapal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes ProjectElizabeth Ormondroyd, Michael P Mackley, Edward Blair, et al.
Current Rheumatology Reports|November 26, 2021
The Musculoskeletal Manifestations of Marfan Syndrome: Diagnosis, Impact, and ManagementLily Pollock, Ashley Ridout, James Teh, et al.
American Journal of Medical Genetics. Part A|May 16, 2015
ADAMTSL4-associated isolated ectopia lentis: Further patients, novel mutations and a detailed phenotype descriptionTeresa M Neuhann, Annette Stegerer, Angelika Riess, et al.
Pageof 7

Showing results (11-20 of 67) with videos related to

Sort By:
Pageof 7
European Journal of Human Genetics : EJHG|February 15, 2018
Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative studyMichael P Mackley, Edward Blair, Michael Parker, et al.
Obstetric Medicine|May 17, 2021
Loeys-Dietz syndrome in pregnancyKatharine E Thomas, Jennifer Hogan, Alex Pitcher, et al.
Microbes and Infection|September 24, 2004
Recombinant respiratory syncytial virus lacking secreted glycoprotein G is attenuated, non-pathogenic but induces protective immunityCaroline F Maher, Tracy Hussell, Edward Blair, et al.
European Journal of Human Genetics : EJHG|June 13, 2019
Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular diseaseJames Buchanan, Edward Blair, Kate L Thomson, et al.
European Heart Journal|March 20, 2010
DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness modelSarah Wordsworth, José Leal, Edward Blair, et al.
Respiration; International Review of Thoracic Diseases|September 26, 2012
The impact of obstructive sleep apnea on aortic disease in Marfan's syndromeMalcolm Kohler, Alex Pitcher, Edward Blair, et al.
Developmental Medicine and Child Neurology|November 22, 2011
Early use of high-dose riboflavin in a case of Brown-Vialetto-Van Laere syndromeGeetha Anand, Nadeem Hasan, Sathiya Jayapal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes ProjectElizabeth Ormondroyd, Michael P Mackley, Edward Blair, et al.
Current Rheumatology Reports|November 26, 2021
The Musculoskeletal Manifestations of Marfan Syndrome: Diagnosis, Impact, and ManagementLily Pollock, Ashley Ridout, James Teh, et al.
American Journal of Medical Genetics. Part A|May 16, 2015
ADAMTSL4-associated isolated ectopia lentis: Further patients, novel mutations and a detailed phenotype descriptionTeresa M Neuhann, Annette Stegerer, Angelika Riess, et al.
Pageof 7