HuGE Literature Finder
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Coronal craniosynostosis due to TCF12 mutations in patients from Turkey. American journal of medical genetics. Part A 2019 Jul . Yilmaz Elanur, Mihci Ercan, Nur Banu, Alper Ozgul |
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. Nature genetics 2013 Jan . Sharma VP, Fenwick AL, Brockop MS, McGowan SJ, Goos JA, Hoogeboom AJ, Brady AF, Jeelani NO, Lynch SA, Mulliken JB, Murray DJ, Phipps JM, Sweeney E, Tomkins SE, Wilson LC, Bennett S, Cornall RJ, Broxholme J, Kanapin A, Johnson D, Wall SA, van der Spek PJ, Mathijssen IM, Maxson RE, Twigg SR, Wilkie AO |
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