Author:
Ma Hong Wi,Lajeunie Elisabeth,Le Merrer Martine,de Parseval Nathalie,Serville Françoise,Weissenbach Jean,Munnich Arnold,Renier Dominique
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference13 articles.
1. Cohen MM Jr (1986) Syndromes with craniosynostosis. In: Cohen MM Jr (ed) Craniosynostosis. Diagnosis, evaluation, and management. Raven Press, New York, pp 413?590
2. Crouzon O (1912) Dysostose cranio-faciale héréditaire. Bull Soc Med Hôp Paris 33:545?555
3. Gorlin RJ, Cohen MM Jr, Levin LS (1990) Syndromes of the head and neck, 3rd edn. McGraw-Hill, New York, pp 524?626
4. Jabs EW, Li X, Scott AF, Meyers G, Chen W, Eccles M, Mao J, Charnas LR, Jackson CE, Jayle M (1994) Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nature Genet 8:275?279
5. Lajeunie E, Ma HW, Bonaventure J, Munnich A, Le Merrer M, Renier D (1995) FGFR2 mutations in Pfeiffer syndrome. Nature Genet 9:108
Cited by
17 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