E-mail a Wiley Online Library Link

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

Version of Record online: 4 JUN 2012 | DOI: 10.1111/j.1399-0004.2012.01890.x

Complete the form below and we will send an e-mail message containing a link to the selected article on your behalf

Required = Required Field