Mutations of TCF12, encoding a basic-helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

✍ Scribed by Sharma, Vikram P; Fenwick, Aimée L; Brockop, Mia S; McGowan, Simon J; Goos, Jacqueline AC; Hoogeboom, A Jeannette M; Brady, Angela F; Jeelani, Owase; Lynch, Sally Ann; Mulliken, John B; Murray, Dylan J; Phipps, Julie M; Sweeney, Elizabeth; Tomkins, Susan E; Wilson, Louise C; Bennett, Sophia; Cornall, Richard J; Broxholme, John; Kanapin, Alexander; Donnelly, Peter; Johnson, David; Wall, Steven A; van der Spek, Peter J; Mathijssen, Irene MJ; Maxson, Robert E; Twigg, Stephen RF; Wilkie, Andrew OM

• Book ID: 121460903
• Publisher: The Lancet
• Year: 2013
• Tongue: English
• Weight: 56 KB
• Volume: 381
• Category: Article
• ISSN: 0140-6736
• DOI: 10.1016/S0140-6736(13)60554-1