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article scientifique vetenskaplig artikel artigo científico tieteellinen artikkeli 2010年学术文章 artigo científico научни чланак επιστημονικό άρθρο 2010年学术文章 wissenschaftlicher Artikel articolo scientifico scientific article published on 14 October 2010 2010年學術文章 artículo científico publicado en 2010 научная статья bài báo khoa học article scientific 2010年学术文章 מאמר מדעי 2010年學術文章 vitskapeleg artikkel ১৪ অক্টোবর ২০১০-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ scienca artikolo artikulong pang-agham 2010年學術文章 мақолаи илмӣ scientific article published on 14 October 2010 2010年学术文章 2010年の論文 wetenschappelijk artikel vědecký článek article científic научни чланак наукова стаття, опублікована в жовтні 2010 videnskabelig artikel bilimsel makale artículu científicu 2010年學術文章 artykuł naukowy научна статия teaduslik artikkel artigo científico vitenskapelig artikkel vedecký článok 2010年学术文章 مقالة علمية نشرت في 14 أكتوبر 2010 2010年学术文章 บทความทางวิทยาศาสตร์ artikull shkencor 2010년 논문 naučni članak articol științific tudományos cikk 2010 nî lūn-bûn სამეცნიერო სტატია scientific article published on 14 October 2010 2010年學術文章 artikel ilmiah
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Implementation of array based whole-genome high-resolution technologies confirms the absence of secondary copy-number alterations in MLL-AF4-positive infant ALL patients. Implementation of array based whole-genome high-resolution technologies confirms the absence of secondary copy-number alterations in MLL-AF4-positive infant ALL patients.
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Implementation of array based whole-genome high-resolution technologies confirms the absence of secondary copy-number alterations in MLL-AF4-positive infant ALL patients. Implementation of array based whole-genome high-resolution technologies confirms the absence of secondary copy-number alterations in MLL-AF4-positive infant ALL patients.
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Implementation of array based whole-genome high-resolution technologies confirms the absence of secondary copy-number alterations in MLL-AF4-positive infant ALL patients. Implementation of array based whole-genome high-resolution technologies confirms the absence of secondary copy-number alterations in MLL-AF4-positive infant ALL patients.
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Implementation of array based whole-genome high-resolution technologies confirms the absence of secondary copy-number alterations in MLL-AF4-positive infant ALL patients.
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