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Sarah T. South, Heidi Whitby, Teresa Maxwell, Emily Aston, Arthur R. Brothman and John C. Carey Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf–Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith–Wiedemann or Russell–Silver phenotype American Journal of Medical Genetics Part A 146A

Version of Record online: 16 SEP 2008 | DOI: 10.1002/ajmg.a.32516

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