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F F Hamdan, H Daoud, L Patry, A Dionne-Laporte, D Spiegelman, S Dobrzeniecka, G A Rouleau and J L Michaud Parent–child exome sequencing identifiesa de novo truncating mutation in TCF4 in non-syndromic intellectual disability Clinical Genetics 83

Article first published online: 4 JUN 2012 | DOI: 10.1111/j.1399-0004.2012.01890.x

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