Pathology in metopic synostosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00381-013-2284-4.pdf
Reference58 articles.
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2. Vissers LELM, Cox TC, Maga AM, Short KM, Wiradjaja F, Janssen IM, Jehee F, Bertola D, Liu J, Yagnik G, Sekiguchi K, Kiyozumi D, Bokhoven H, Marcelis C, Cunningham ML, Anderson PJ, Boyadjiev SA, Passos-Bueno MR, Veltman JA, Smyth I, Buckley MF, Roscioli T (2011) Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice. PLOS Genet 7(9):e1002278
3. Patel A, Terner J, Travieso R, Clune JE, Steinbacher D, Persing JA (2012) On Bernard Sarnat's 100th birthday: pathology and management of craniosynostosis. J Craniofac Surg 23(1):105–112
4. Vu HL, Panchal J, Parker EE, Levine NS, Francel P (2001) The timing of physiologic closure of the metopic suture: a review of 159 patients using reconstructed 3D CT scans of the craniofacial region. J Craniofac Surg 12(6):527–532
5. Cohen MM Jr (2012) No man's craniosynostosis: the arcana of sutural knowledge. J Craniofac Surg 23(1):338–342
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