Author:
Anderson Peter J.,Netherway David J.,Abbott Amanda H.,Cox Timothy,Roscioli Tony,David David J.
Subject
Neurology (clinical),General Medicine,Surgery,Pediatrics, Perinatology and Child Health
Reference10 articles.
1. Cohen MM Jr: Apert syndrome; in Cohen MM Jr, McLean RE (eds): Craniosynostosis: Diagnosis, Evaluation and Management, ed 2. New York, Oxford University Press, 2000, pp 316-353.
2. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
3. Clinical variability in patients with Apert's syndrome
Cited by
22 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献