Concerning an Applicant for Narcotic Medication

nork Blair, Edward
Argitaratua 1940

Concerning an Applicant for Narcotic Medication

nork Blair, Edward
Argitaratua 1940

Aligning the Economic Value of Companion Diagnostics and Stratified Medicines

nork Blair, Edward D., Stratton, Elyse K., Kaufmann, Martina
Argitaratua izan da J Pers Med (2012)

Effective cascade screening through identification of a mutation in RYR2 in a large family with a history of sudden death

nork Bailey, Claire, Blair, Edward, Garratt, Clifford, Newman, William G.
Argitaratua izan da J Cardiol Cases (2015)

Initial Binding of Murine Leukemia Virus Particles to Cells Does Not Require Specific Env-Receptor Interaction

nork Pizzato, Massimo, Marlow, Susan A., Blair, Edward D., Takeuchi, Yasuhiro
Argitaratua 1999

Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications

nork Ormondroyd, Elizabeth, Oates, Stephanie, Parker, Michael, Blair, Edward, Watkins, Hugh
Argitaratua 2014

Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study

nork Mackley, Michael P, Blair, Edward, Parker, Michael, Taylor, Jenny C, Watkins, Hugh, Ormondroyd, Elizabeth
Argitaratua izan da Eur J Hum Genet (2018)

Loeys–Dietz syndrome in pregnancy

nork Thomas, Katharine E, Hogan, Jennifer, Pitcher, Alex, Mackillop, Lucy, Blair, Edward, Frise, Charlotte J
Argitaratua izan da Obstet Med (2019)

Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular disease

nork Buchanan, James, Blair, Edward, Thomson, Kate L., Ormondroyd, Elizabeth, Watkins, Hugh, Taylor, Jenny C., Wordsworth, Sarah
Argitaratua izan da Eur J Hum Genet (2019)

“Not pathogenic until proven otherwise”: perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and th...

nork Ormondroyd, Elizabeth, Mackley, Michael P, Blair, Edward, Craft, Judith, Knight, Julian C, Taylor, Jenny C, Taylor, John, Watkins, Hugh
Argitaratua izan da Genet Med (2017)

Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study

nork Ormondroyd, Elizabeth, Mackley, Michael P, Blair, Edward, Craft, Jude, Knight, Julian C, Taylor, John, Taylor, Jenny C, Wilkie, Andrew OM, Watkins, Hugh
Argitaratua izan da Eur J Hum Genet (2017)

Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom

nork Wordsworth, Sarah, Buchanan, James, Regan, Regina, Davison, Val, Smith, Kim, Dyer, Sara, Campbell, Carolyn, Blair, Edward, Maher, Eddy, Taylor, Jenny, Knight, Samantha J. L.
Argitaratua 2007

Aortic dissection: visualisation of aortic blood flow and quantification of wall shear stress using time-resolved, 3D phase-contrast MRI

nork Pitcher, Alex, Cassar, Tom E, Leeson, Paul, Francis, Jane M, Blair, Edward, Wordsworth, Paul B, Forfar, J Colin, Petersen, Steffen E, Markl, Michael, Neubauer, Stefan
Argitaratua 2011

Human Slack potassium channel mutations increase positive cooperativity between individual channels

nork Kim, Grace E., Kronengold, Jack, Barcia, Giulia, Quraishi, Imran H., Martin, Hilary C., Blair, Edward, Taylor, Jenny C., Dulac, Olivier, Colleaux, Laurence, Nabbout, Rima, Kaczmarek, Leonard K.
Argitaratua izan da Cell Rep (2014)

Visualisation of aortic flow disturbance in Marfan syndrome by 4D phase-contrast CMR

nork Pitcher, Alex, Cassar, Tom E, Suttie, Joseph, Francis, Jane M, Leeson, Paul, Blair, Edward, Wordsworth, B Paul, Forfar, J Colin, Myerson, Saul G, Markl, Michael, Neubauer, Stefan, Petersen, Steffen E
Argitaratua 2011

New insights into the pathogenesis of autosomal dominant cutis laxa with report of five ELN mutations

nork Callewaert, Bert, Renard, Marjolijn, Hucthagowder, Vishwanathan, Albrecht, Beate, Hausser, Ingrid, Blair, Edward, Dias, Cristina, Albino, Alice, Wachi, Hiroshi, Sato, Fumiaki, Mecham, Robert P., Loeys, Bart, Coucke, Paul J., De Paepe, Anne, Urban, Zsolt
Argitaratua 2011

Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE

nork Kienzler, Anne-Kathrin, van Schouwenburg, Pauline A., Taylor, John, Marwah, Ishita, Sharma, Richa U., Noakes, Charlotte, Thomson, Kate, Sadler, Ross, Segal, Shelley, Ferry, Berne, Taylor, Jenny C., Blair, Edward, Chapel, Helen, Patel, Smita Y.
Argitaratua izan da Clin Immunol (2016)

A meckelin–filamin A interaction mediates ciliogenesis

nork Adams, Matthew, Simms, Roslyn J., Abdelhamed, Zakia, Dawe, Helen R., Szymanska, Katarzyna, Logan, Clare V., Wheway, Gabrielle, Pitt, Eva, Gull, Keith, Knowles, Margaret A., Blair, Edward, Cross, Sally H., Sayer, John A., Johnson, Colin A.
Argitaratua 2012

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma

nork Bayley, Jean-Pierre, van Minderhout, Ivonne, Weiss, Marjan M, Jansen, Jeroen C, Oomen, Peter HN, Menko, Fred H, Pasini, Barbara, Ferrando, Barbara, Wong, Nora, Alpert, Lesley C, Williams, Rosie, Blair, Edward, Devilee, Peter, Taschner, Peter EM
Argitaratua 2006

Prenatal Diagnosis of Congenital Adrenal Hyperplasia Caused by P450 Oxidoreductase Deficiency

nork Reisch, Nicole, Idkowiak, Jan, Hughes, Beverly A., Ivison, Hannah E., Abdul-Rahman, Omar A., Hendon, Laura G., Olney, Ann Haskins, Nielsen, Shelly, Harrison, Rachel, Blair, Edward M., Dhir, Vivek, Krone, Nils, Shackleton, Cedric H. L., Arlt, Wiebke
Argitaratua 2013