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1دورية أكاديمية
المؤلفون: L A Hughes, K McKay-Bounford, E A Webb, P Dasani, S Clokie, H Chandran, L McCarthy, Z Mohamed, J M W Kirk, N P Krone, S Allen, T R P Cole
المصدر: Endocrine Connections, Vol 8, Iss 2, Pp 100-111 (2019)
مصطلحات موضوعية: next generation sequencing (NGS), disorders of sex development (DSD), gene, variant, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
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المؤلفون: Lucy Loong, Cankut Cubuk, Subin Choi, Sophie Allen, Beth Torr, Alice Garrett, Chey Loveday, Miranda Durkie, Alison Callaway, George J. Burghel, James Drummond, Rachel Robinson, Ian R. Berry, Andrew Wallace, Diana M. Eccles, Marc Tischkowitz, Sian Ellard, James S. Ware, Helen Hanson, Clare Turnbull, S. Samant, A. Lucassen, A. Znaczko, A. Shaw, A. Ansari, A. Kumar, A. Donaldson, A. Murray, A. Ross, A. Taylor-Beadling, A. Taylor, A. Innes, A. Brady, A. Kulkarni, A.-C. Hogg, A. Ramsay Bowden, A. Hadonou, B. Coad, B. McIldowie, B. Speight, B. DeSouza, B. Mullaney, C. McKenna, C. Brewer, C. Olimpio, C. Clabby, C. Crosby, C. Jenkins, C. Armstrong, C. Bowles, C. Brooks, C. Byrne, C. Maurer, D. Baralle, D. Chubb, D. Stobo, D. Moore, D. O'Sullivan, D. Donnelly, D. Randhawa, D. Halliday, E. Atkinson, E. Baple, E. Rauter, E. Johnston, E. Woodward, E. Maher, E. Sofianopoulou, E. Petrides, F. Lalloo, F. McRonald, F. Pelz, I. Frayling, G. Evans, G. Corbett, G. Rea, H. Clouston, H. Powell, H. Williamson, H. Carley, H.J.W. Thomas, I. Tomlinson, J. Cook, J. Hoyle, J. Tellez, J. Whitworth, J. Williams, J. Murray, J. Campbell, J. Tolmie, J. Field, J. Mason, J. Burn, J. Bruty, J. Callaway, J. Grant, J. Del Rey Jimenez, J. Pagan, J. VanCampen, J. Barwell, K. Monahan, K. Tatton-Brown, K.-R. Ong, K. Murphy, K. Andrews, K. Mokretar, K. Cadoo, K. Smith, K. Baker, K. Brown, K. Reay, K. McKay Bounford, K. Bradshaw, K. Russell, K. Stone, K. Snape, L. Crookes, L. Reed, L. Taggart, L. Yarram, L. Cobbold, L. Walker, L. Hawkes, L. Busby, L. Izatt, L. Kiely, L. Hughes, L. Side, L. Sarkies, K.-L. Greenhalgh, M. Shanmugasundaram, M. Duff, M. Bartlett, M. Watson, M. Owens, M. Bradford, M. Huxley, M. Slean, M. Ryten, M. Smith, M. Ahmed, N. Roberts, C. O'Brien, O. Middleton, P. Tarpey, P. Logan, P. Dean, P. May, P. Brace, R. Tredwell, R. Harrison, R. Hart, R. Kirk, R. Martin, R. Nyanhete, R. Wright, R. Davidson, R. Cleaver, S. Talukdar, S. Butler, J. Sampson, S. Ribeiro, S. Dell, S. Mackenzie, S. Hegarty, S. Albaba, S. McKee, S. Palmer-Smith, S. Heggarty, S. MacParland, S. Greville-Heygate, S. Daniels, S. Prapa, S. Abbs, S. Tennant, S. Hardy, S. MacMahon, T. McVeigh, T. Foo, T. Bedenham, T. Cranston, T. McDevitt, V. Clowes, V. Tripathi, V. McConnell, N. Woodwaer, Y. Wallis, Z. Kemp, G. Mullan, L. Pierson, L. Rainey, C. Joyce, A. Timbs, A.-M. Reuther, B. Frugtniet, C. Husher, C. Lawn, C. Corbett, D. Nocera-Jijon, D. Reay, E. Cross, F. Ryan, H. Lindsay, J. Oliver, J. Dring, J. Spiers, J. Harper, K. Ciucias, L. Connolly, M. Tsang, R. Brown, S. Shepherd, S. Begum, T. Tadiso, T. Linton-Willoughby, H. Heppell, K. Sahan, L. Worrillow, Z. Allen, M. Barlett, C. Watt, M. Hegarty
المساهمون: British Heart Foundation, Wellcome Trust
المصدر: Loong, L, Cubuk, C, Choi, S, Allen, S, Torr, B, Garrett, A, Loveday, C, Durkie, M, Callaway, A, Burghel, GJ, Drummond, J, Robinson, R, Berry, IR, Wallace, A & CanVIG-UK 2021, ' Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants. ', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 24, no. 3, pp. 552-563 . https://doi.org/10.1016/j.gim.2021.11.011
مصطلحات موضوعية: Concordance, Mutation, Missense, Biology, PM5, CanVIG-UK, Humans, Missense mutation, Genetic Predisposition to Disease, Variant, Codon, Genetics (clinical), Genetics, Genetics & Heredity, 0604 Genetics, BRCA1 Protein, Genetic Variation, 1103 Clinical Sciences, Pathogenicity, Classification, MutS Homolog 2 Protein, Genetic Variation/genetics, Mutation, Missense/genetics, MSH2, ACMG, BRCA1 Protein/genetics, MutS Homolog 2 Protein/genetics
وصف الملف: text
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a638418e559b935daf78b3ef4e1f05a
http://hdl.handle.net/10044/1/95227 -
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المؤلفون: Nils Krone, Liam McCarthy, Harish Chandran, Trevor Cole, Zainaba Mohamed, Samuel Clokie, P Dasani, Jeremy Kirk, K McKay-Bounford, Lowri Hughes, Stephanie Allen, E A Webb
المصدر: Endocrine Connections
Endocrine Connections, Vol 8, Iss 2, Pp 100-111 (2019)مصطلحات موضوعية: lcsh:RC648-665, medicine.diagnostic_test, disorders of sex development (DSD), business.industry, Endocrinology, Diabetes and Metabolism, Research, Inheritance (genetic algorithm), next generation sequencing (NGS), Bioinformatics, medicine.disease, lcsh:Diseases of the endocrine glands. Clinical endocrinology, DNA sequencing, Patient management, Endocrinology, variant, Internal Medicine, Medicine, Disorders of sex development, Medical diagnosis, Genetic diagnosis, business, gene, Uncertain significance, Genetic testing
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::777eafcceaa556fe92c13a0f78da7806
http://europepmc.org/articles/PMC6373624 -
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المؤلفون: Paul Gissen, K. McKay Bounford
المصدر: Journal of Neurology
مصطلحات موضوعية: Pathology, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Clinical Neurology, Vesicular Transport Proteins, Review, Biology, Gene mutation, medicine.disease_cause, chemistry.chemical_compound, Niemann-Pick C1 Protein, hemic and lymphatic diseases, Diagnosis, medicine, Genetics, Humans, Genetic Testing, Genetic testing, Glycoproteins, Mutation, Niemann–Pick disease, type C, Membrane Glycoproteins, medicine.diagnostic_test, Cholesterol, Incidence (epidemiology), Intracellular Signaling Peptides and Proteins, nutritional and metabolic diseases, Niemann-Pick Disease, Type C, medicine.disease, NPC2, 3. Good health, Staining, NPC1, chemistry, Neurology, Neurology (clinical), Niemann Pick type C disease (NP-C), Carrier Proteins
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7دورية أكاديمية
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