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RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family by Elisangela P. S. Quedas, Viviane C. Longuini, Tomoko Sekiya, Flavia L. Coutinho, Sergio P. A. Toledo, Uenis Tannuri, Rodrigo A. Toledo
Published 2012-01-01
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