Parent–child exome sequencing identifiesa de novo truncating mutation in TCF4 in non-syndromic intellectual disability

✍ Scribed by F F Hamdan; H Daoud; L Patry; A Dionne-Laporte; D Spiegelman; S Dobrzeniecka; G A Rouleau; J L Michaud

• Book ID: 119981563
• Publisher: John Wiley and Sons
• Year: 2012
• Tongue: English
• Weight: 684 KB
• Volume: 83
• Category: Article
• ISSN: 0009-9163
• DOI: 10.1111/j.1399-0004.2012.01890.x