Хайлтын үр дүнгүүд - Blair, Edward

Concerning an Applicant for Narcotic Medication -н Blair, Edward

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Concerning an Applicant for Narcotic Medication -н Blair, Edward

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Aligning the Economic Value of Companion Diagnostics and Stratified Medicines -н Blair, Edward D., Stratton, Elyse K., Kaufmann, Martina

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Effective cascade screening through identification of a mutation in RYR2 in a large family with a history of sudden death -н Bailey, Claire, Blair, Edward, Garratt, Clifford, Newman, William G.

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Initial Binding of Murine Leukemia Virus Particles to Cells Does Not Require Specific Env-Receptor Interaction -н Pizzato, Massimo, Marlow, Susan A., Blair, Edward D., Takeuchi, Yasuhiro

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Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications -н Ormondroyd, Elizabeth, Oates, Stephanie, Parker, Michael, Blair, Edward, Watkins, Hugh

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Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study -н Mackley, Michael P, Blair, Edward, Parker, Michael, Taylor, Jenny C, Watkins, Hugh, Ormondroyd, Elizabeth

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Loeys–Dietz syndrome in pregnancy -н Thomas, Katharine E, Hogan, Jennifer, Pitcher, Alex, Mackillop, Lucy, Blair, Edward, Frise, Charlotte J

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Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular disease -н Buchanan, James, Blair, Edward, Thomson, Kate L., Ormondroyd, Elizabeth, Watkins, Hugh, Taylor, Jenny C., Wordsworth, Sarah

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“Not pathogenic until proven otherwise”: perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and th... -н Ormondroyd, Elizabeth, Mackley, Michael P, Blair, Edward, Craft, Judith, Knight, Julian C, Taylor, Jenny C, Taylor, John, Watkins, Hugh

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The Musculoskeletal Manifestations of Marfan Syndrome: Diagnosis, Impact, and Management -н Pollock, Lily, Ridout, Ashley, Teh, James, Nnadi, Colin, Stavroulias, Dionisios, Pitcher, Alex, Blair, Edward, Wordsworth, Paul, Vincent, Tonia L.

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Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study -н Ormondroyd, Elizabeth, Mackley, Michael P, Blair, Edward, Craft, Jude, Knight, Julian C, Taylor, John, Taylor, Jenny C, Wilkie, Andrew OM, Watkins, Hugh

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Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom -н Wordsworth, Sarah, Buchanan, James, Regan, Regina, Davison, Val, Smith, Kim, Dyer, Sara, Campbell, Carolyn, Blair, Edward, Maher, Eddy, Taylor, Jenny, Knight, Samantha J. L.

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

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Human Slack potassium channel mutations increase positive cooperativity between individual channels -н 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.

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

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

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

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A meckelin–filamin A interaction mediates ciliogenesis -н 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.

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

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