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Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects Johnson, Ben; Lowe, Gillian C.; Futterer, Jane; Lordkipanidze, Marie; MacDonald, David; Simpson, Michael A.; Sanchez-Guiu, Isabel; Drake, Sian; Bem, Danai; Leo, Vincenzo; Fletcher, Sarah J.; Dawood, Ban; Rivera, Jose; Allsup, David; Biss, Tina; Bolton-Maggs, Paula H. B.; Collins, Peter; Curry, Nicola; Grimley, Charlotte; James, Beki; Makris, Mike; Motwani, Jayashree; Pavord, Sue; Talks, Katherine; Thachil, Jecko; Wilde, Jonathan; Williams, Mike; Harrison, Paul; Gissen, Paul; Mundell, Stuart; Mumford, Andrew; Daly, Martina E.; Watson, Steve P.; Morgan, Neil V. 分享 收藏
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Use of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders Leo, V. C.; Morgan, N. V.; Bem, D.; Jones, M. L.; Lowe, G. C.; Lordkipanidze, M.; Drake, S.; Simpson, M. A.; Gissen, P.; Mumford, A.; Watson, S. P.; Daly, M. E. 分享 收藏
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ASSOCIATION BETWEEN A POLYMORPHISM IN THE FRACTALKINE RECEPTOR, CX3CR1, AND RHEUMATOID ARTHRITIS Stack, J.; Hegarty, K.; Murphy, G.; O'Sullivan, M.; Fanning, L.; Healy, L.; Daly, M.; Harney, S.; Shanahan, F.; Molloy, M. 分享 收藏
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