檢索結果 - Patrick J. Morrison

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  1. 1
    Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome).

    Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome). 由 Patrick J. Morrison, N C Nevin

    出版 1996
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    Revisão
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  2. 2
    Epidemiology, Clinical Features, and Genetics of Multiple Endocrine Neoplasia Type 2B in a Complete Population

    Epidemiology, Clinical Features, and Genetics of Multiple Endocrine Neoplasia Type 2B in a Complete Population 由 Anna Znaczko, Deirdre E. Donnelly, Patrick J. Morrison

    出版 2014
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    Artigo
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  3. 3
    The Impact of Neurofibromatosis Type 1 on the Health and Wellbeing of Australian Adults

    The Impact of Neurofibromatosis Type 1 on the Health and Wellbeing of Australian Adults 由 Hilda Crawford, Belinda Barton, Meredith Wilson, Yemima Berman, Valerie J. McKelvey‐Martin, Patrick J. Morrison, Kathryn N. North

    出版 2015
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    Artigo
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  4. 4
    Predictive genetic testing for BRCA1/2 in a UK clinical cohort: three-year follow-up

    Predictive genetic testing for BRCA1/2 in a UK clinical cohort: three-year follow-up 由 Claire Foster, Maggie Watson, Rosalind A. Eeles, Diana Eccles, S. Ashley, R Davidson, James Mackay, Patrick J. Morrison, Penelope Hopwood, D. Gareth Evans

    出版 2007
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    Artigo
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  5. 5
    ORG 10172: a low molecular weight heparinoid anticoagulant with a long half‐life in man.

    ORG 10172: a low molecular weight heparinoid anticoagulant with a long half‐life in man. 由 ID Bradbrook, HN Magnani, H.C.T. Moelker, Patrick J. Morrison, John W. Robinson, HJ Rogers, Spector Rg, T Van Dinther, H. P. Wijnand

    出版 1987
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  6. 6
    Psychosocial impact of breast/ovarian (BRCA 1/2) cancer-predictive genetic testing in a UK multi-centre clinical cohort

    Psychosocial impact of breast/ovarian (BRCA 1/2) cancer-predictive genetic testing in a UK multi-centre clinical cohort 由 Maggie Watson, Claire Foster, Rosalind A. Eeles, Diana Eccles, Sue Ashley, R Davidson, James Mackay, Patrick J. Morrison, Penelope Hopwood, D. Gareth Evans

    出版 2004
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  7. 7
    Predictive testing for BRCA1/2: attributes, risk perception and management in a multi-centre clinical cohort

    Predictive testing for BRCA1/2: attributes, risk perception and management in a multi-centre clinical cohort 由 Claire Foster, D. Gareth Evans, Rosalind A. Eeles, Diana Eccles, Sue Ashley, Lucy Brooks, R Davidson, James Mackay, Patrick J. Morrison, Maggie Watson

    出版 2002
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    Artigo
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  8. 8
    Genetic professionals' reports of nondisclosure of genetic risk information within families

    Genetic professionals' reports of nondisclosure of genetic risk information within families 由 Angus Clarke, Martin Richards, L Kerzin-Storrar, Jane Halliday, Mary Young, Sheila A Simpson, Katie Featherstone, Karen Forrest, Anneke Lucassen, Patrick J. Morrison, Oliver Quarrell, Helen Stewart

    出版 2005
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  9. 9
    Recurrence risk of congenital malformations in infants exposed to antiepileptic drugs in utero

    Recurrence risk of congenital malformations in infants exposed to antiepileptic drugs in utero 由 Ellen Campbell, Emma Devenney, Jim Morrow, Aline Russell, W. Henry Smithson, Linda M. Parsons, Iain G. C. Robertson, Beth Irwin, Patrick J. Morrison, Stephen J. Hunt, John Craig

    出版 2012
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    Artigo
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  10. 10
    Valproate and the risk for congenital malformations: Is formulation and dosage regime important?

    Valproate and the risk for congenital malformations: Is formulation and dosage regime important? 由 E. Mawhinney, Jacqueline Campbell, John Craig, Ailsa Russell, W Henry Smithson, Linda M. Parsons, Ian Robertson, B. Irwin, Patrick J. Morrison, Brenda Liggan, N Delanty, S. Hunt, Jim Morrow

    出版 2012
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  11. 11
    Clinical Experience in the Screening and Management of a Large Kindred With Familial Isolated Pituitary Adenoma Due to an Aryl Hydrocarbon Receptor Interacting Protein (AIP) Mutation

    Clinical Experience in the Screening and Management of a Large Kindred With Familial Isolated Pituitary Adenoma Due to an Aryl Hydrocarbon Receptor Interacting Protein (AIP) Mutati... 由 Fred Williams, Steven Hunter, Lisa Bradley, Harvinder Chahal, Helen L. Storr, Scott Akker, Ajith Kumar, Stephen M. Orme, Jane Evanson, Noina Abid, Patrick J. Morrison, Márta Korbonits, A. Brew Atkinson

    出版 2013
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    Artigo
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  12. 12
    Current policies for surveillance and management in women at risk of breast and ovarian cancer: a survey among 16 European family cancer clinics

    Current policies for surveillance and management in women at risk of breast and ovarian cancer: a survey among 16 European family cancer clinics 由 Hans F. A. Vasen, N E Haites, D. Gareth Evans, C. M. Steel, Pål Møller, Shirley Hodgson, Diana Eccles, Patrick J. Morrison, Dominique Stoppa Lyonet, Jenny Chang‐Claude, Maria A. Caligo

    出版 1998
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  13. 13
    Changing antiepilepsy drug-prescribing trends in women with epilepsy in the UK and Ireland and the impact on major congenital malformations

    Changing antiepilepsy drug-prescribing trends in women with epilepsy in the UK and Ireland and the impact on major congenital malformations 由 Michael Kinney, James Morrow, C. C. Patterson, Ellen Campbell, Aline Russell, Henry Smithson, Linda M. Parsons, Patrick J. Morrison, Rebecca Bromley, Brenda Liggan, Norman Delanty, Beth Irwin, Stephen J. Hunt, John Craig

    出版 2018
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  14. 14
    Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3

    Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3 由 M. Andrew Nesbit, Fadil Hannan, Sarah Howles, Adam J. Reed, Treena Cranston, Clare Thakker, Lorna Gregory, Andrew J. Rimmer, Nigel Rust, Una Graham, Patrick J. Morrison, Steven Hunter, Michael P. Whyte, Gil McVean, David Buck, Rajesh V. Thakker

    出版 2012
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  15. 15
    Germline BHD-Mutation Spectrum and Phenotype Analysis of a Large Cohort of Families with Birt-Hogg-Dubé Syndrome

    Germline BHD-Mutation Spectrum and Phenotype Analysis of a Large Cohort of Families with Birt-Hogg-Dubé Syndrome 由 Laura S. Schmidt, Michael L. Nickerson, Michelle B. Warren, G.M. Glenn, Jorge R. Toro, Maria J. Merino, Maria L. Turner, Peter L. Choyke, Nirmala Sharma, James Peterson, Patrick J. Morrison, Eamonn R. Maher, McClellan M. Walther, Berton Zbar, W. Marston Linehan

    出版 2005
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    Artigo
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  16. 16
    <i>AIP</i>Mutation in Pituitary Adenomas in the 18th Century and Today

    <i>AIP</i>Mutation in Pituitary Adenomas in the 18th Century and Today 由 Harvinder Chahal, Karen Stals, Martina Unterländer, David J. Balding, Mark Thomas, Ajith Kumar, G. M. Besser, A. Brew Atkinson, Patrick J. Morrison, Trevor A. Howlett, Miles Levy, Steve Orme, Scott Akker, Richard L. Abel, Ashley Grossman, Joachim Bürger, Sian Ellard, Márta Korbonits

    出版 2011
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  17. 17
    BRCA1 and c-Myc Associate to Transcriptionally Repress Psoriasin, a DNA Damage–Inducible Gene

    BRCA1 and c-Myc Associate to Transcriptionally Repress Psoriasin, a DNA Damage–Inducible Gene 由 Richard D. Kennedy, Julia J. Gorski, Jennifer E. Quinn, Gail E. Stewart, Colin R. James, Stephen P.G. Moore, Karl Mulligan, Ethan Emberley, T F Lioe, Patrick J. Morrison, Paul B. Mullan, George Reid, Patrick G. Johnston, Peter H. Watson, D. Paul Harkin

    出版 2005
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  18. 18
    Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study

    Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study 由 Oliver Quarrell, Alan S. Rigby, L Barron, Yanick J. Crow, A. Dalton, N R Dennis, Alan Fryer, Frances Heydon, Esther Kinning, Alison Lashwood, Monique Losekoot, L Margerison, Shannon K. McDonnell, Patrick J. Morrison, Andrew Norman, Michael Peterson, F. Lucy Raymond, Sharon Simpson, Elizabeth Thompson, Jon Warner

    出版 2006
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    Carta
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  19. 19
    A Comprehensive Next Generation Sequencing–Based Genetic Testing Strategy To Improve Diagnosis of Inherited Pheochromocytoma and Paraganglioma

    A Comprehensive Next Generation Sequencing–Based Genetic Testing Strategy To Improve Diagnosis of Inherited Pheochromocytoma and Paraganglioma 由 Eleanor Rattenberry, Lindsey Vialard, Anna C. Y. Yeung, Hayley Bair, Kirsten McKay, Mariam Jafri, Natalie Canham, Trevor Cole, Judit Dénes, Shirley V. Hodgson, Richard Irving, Louise Izatt, Márta Korbonits, Ajith Kumar, Fiona Lalloo, Patrick J. Morrison, Emma R. Woodward, Fiona MacDonald, Yvonne Wallis, Eamonn R. Maher

    出版 2013
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    Artigo
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  20. 20
    Deletions of the PRKAR1A Locus at 17q24.2-q24.3 in Carney Complex: Genotype-Phenotype Correlations and Implications for Genetic Testing

    Deletions of the PRKAR1A Locus at 17q24.2-q24.3 in Carney Complex: Genotype-Phenotype Correlations and Implications for Genetic Testing 由 Calvin Ke, Anélia Horvath, Edra London, Fábio R. Faucz, Annalisa Vetro, Isaac Lévy, Evgenia Gourgari, Andrew Dauber, Ingrid A. Holm, Patrick J. Morrison, Margaret F. Keil, Charalampos Lyssikatos, Eric D. Smith, Marc A. Sanidad, JoAnn C. Kelly, Zunyan Dai, Philip N. Mowrey, Antonella Forlino, Orsetta Zuffardi, Constantine A. Stratakis

    出版 2013
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