المؤلفون: McHenry, CM, Atkinson, AB, Hunter, SJ, Browne, J, Ennis, CN, Henry, J, Sheridan, B, Bell, PM, Cole, BRW, Purvis, JA, Hughes, SM, Morgan, DR, Donaghy, AE, McCrory, RFR, Walker, S, Convery, RP, Hall, PSJ, Taylor, M, Johnston, SD, Wazir, TU, Cairns, AP, Lewis, G, McQuillan, SL, Adgey, CH, Carl, I, Bhat, S, Lakhanpal, A, Lynch, P, Varghese, A, Scott, PJ, Smith, B, Manoharan, G, Johnson, PW, Neill, J, Douglas, H, Richardson, G, Chew, E, Walsh, S, Hanratty, C, Herity, N, Howe, AJ, Graham, UM, Ritchie, CM, McCance, DR, Donnelly, Deirdre E, McConnell, Vivienne PM, Leslie, H, Young, IS, Mullan, KR, Hunter, M, Hedderwick, S, Donnelly, C, Lewis, AS, McCourt, HJ, Boreham, CA, Courtney, CH, McKinley, MC, Murray, LJ, Woodside, JV, McKavanagh, P, Smyth, AI, Donnelly, PM, Hunter, HL, Corbett, JR, Fearon, P, Kinnaird, M, MacNair, S, Fullerton, K, Wiggam, MI

المصدر: The Ulster Medical Journal

مصطلحات موضوعية: The Ulster Society of Internal Medicine: 82nd -84th meetings, 2009-2010, familial, three-generation, phenotypic variation, Sotos syndrome, Abstract

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmc_________::5655d02ef69156a4d50be0c517f59fd4
http://europepmc.org/articles/PMC3229860