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8. A de novo 17q21.2 duplication in a boy with developmental delay and dysmorphic features. Poirsier-Violle C; Abourra A; Baumann C; Perrin L; Capri Y; Mignot C; Passemard S; Drunat S; Verloes A Eur J Med Genet; 2013 Apr; 56(4):226-8. PubMed ID: 23337768 [TBL] [Abstract][Full Text] [Related]
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