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vědecký článek wetenschappelijk artikel vitenskapelig artikkel 2011年論文 artykuł naukowy บทความทางวิทยาศาสตร์ سائنسی مضمون научна статия scienca artikolo 2011年论文 bilimsel makale 2011年論文 artikulong pang-agham ২০১১-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ artículu científicu espublizáu en 2011 مقالهٔ علمی artigo científico (publicado na 2011) articol științific 2011 թուականի Յունիսին հրատարակուած գիտական յօդուած επιστημονικό άρθρο 2011年論文 teaduslik artikkel 2011年论文 mokslinis straipsnis vedecký článok مقالة علمية bài báo khoa học 2011年の論文 2011년 논문 2011年论文 tudományos cikk artigo científico (publicado na 2011) научни чланак scientific article artigo científico videnskabelig artikel (udgivet 2011) article científic מאמר מדעי 2011年论文 artikull shkencor vetenskaplig artikel article scientific научная статья мақолаи илмӣ мақолаи илмӣ naučni članak 2011年论文 wissenschaftlicher Artikel 2011 թվականի հունիսին հրատարակված գիտական հոդված 2011年論文 artículo científico publicado en 2011 научни чланак наукова стаття, опублікована в червні 2011 vitskapeleg artikkel სამეცნიერო სტატია tieteellinen artikkeli 2011 nî lūn-bûn 2011年論文 2011年论文 articolo scientifico article scientifique (publié 2011)
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Roxann G Ingersoll Ophelia Rogers Jarek P Maciejewski Jerry L Spivak Amit Verma Michael A McDevitt Christine O'Keefe Donna M Williams Brady L Stein Alison R Moliterno
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Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes
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Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes
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Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes
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Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes
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