Author:
Herman T E,Sargar K,Siegel M J
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health
Reference6 articles.
1. Vajo Z, Francomano CA, Wilkin DJ . The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis and Crouzon syndrome with acanthosis nigricans. Endocr Rev 2000; 21: 23–39.
2. Schweitzer DN, Graham JM, Lachman RS, Jabs EW, Okajima K, Przylepa KA et al. Subtle radiographic findings of Achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3. Am J Med Genet 2001; 98: 75–91.
3. Arnaud-Lopez L, Fragoso R, Mantilla-Capacho J, Barros-Nunez P . Crouzon with ancanthosis nigricans. Further delineation of the syndrome. Clin Genetic 2007; 72: 405–410.
4. DiRocco F, Collet C, Legeai-Mallet L, Arnaud E, Le Merrer M, Hadj-Rabia S et al. Crouzon syndrome with acanthosis nigricans: a case-based update. Childs Nerv Syst 2011; 27: 349–354.
5. Sharma VP, Wall SA, Lord H, Lester T, Wilkie AOM . Atypical Crouzon syndrome with a novel Cys62Arg mutation in FGFR2 presenting with Sagittal synostosis. Cleft Palate-Craniofacial J 2012; 49: 373–376.
Cited by
6 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