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Authors: Shlien, Adam Baskin, Berivan Achatz, Maria Isabel W. Stavropoulos, Dimitrios J.
Citation: Shlien, Adam et al., A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13.1 Microdeletion Syndromes, American journal of human genetics (Online) AJHG , 87(5), 2010, pp. 631-642
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