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.

MLA

Vajo, Z., et al. “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.” Endocrine Reviews, vol. 21, no. 1, Feb. 2000, pp. 23–39. EBSCOhost, https://doi.org/10.1210/edrv.21.1.0387.

APA

Vajo, Z., Francomano, C. A., & Wilkin, D. J. (2000). 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. Endocrine Reviews, 21(1), 23–39. https://doi.org/10.1210/edrv.21.1.0387

Chicago

Vajo, Z, C A Francomano, and D J Wilkin. 2000. “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.” Endocrine Reviews 21 (1): 23–39. doi:10.1210/edrv.21.1.0387.