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articol științific wissenschaftlicher Artikel tudományos cikk научни чланак научна статия bilimsel makale 2013年论文 article scientific مقالة علمية 2013 թվականի հոտեմբերին հրատարակված գիտական հոդված 2013 nî lūn-bûn artykuł naukowy 2013年论文 bài báo khoa học επιστημονικό άρθρο 2013年論文 teaduslik artikkel article scientifique (publié 2013) 2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած artigo científico (publicado na 2013) artigo científico мақолаи илмӣ 2013年論文 مقالهٔ علمی naučni članak 2013年论文 научная статья 2013年论文 artículo científico publicado en 2013 наукова стаття, опублікована в жовтні 2013 artikull shkencor מאמר מדעי vitenskapelig artikkel videnskabelig artikel (udgivet 2013) vetenskaplig artikel ২০১৩-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ article científic scienca artikolo სამეცნიერო სტატია 2013年論文 artículu científicu espublizáu en 2013 vitskapeleg artikkel 2013年の論文 vědecký článek scientific article 2013年论文 บทความทางวิทยาศาสตร์ 2013年论文 мақолаи илмӣ 2013年論文 научни чланак tieteellinen artikkeli artigo científico (publicado na 2013) vedecký článok سائنسی مضمون 2013年論文 articolo scientifico mokslinis straipsnis wetenschappelijk artikel 2013년 논문 artikulong pang-agham
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Katherine Talks Jonathan T Wilde Martina E Daly Kirsty Macfarlane Jayashree Motwani Vincenzo C Leo Ban Dawood Danai Bem Peter W Collins Michael Makris Kevin Horner Gillian C Lowe UK Genotyping and Phenotyping of Platelets Study Group
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Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects
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Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects
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