APA (7th ed.) Citation

El-Bazzal, L., Atkinson, A., Gillart, A., Obeid, M., Delague, V., & Mégarbané, A. (2019). A novel EXT2 mutation in a consanguineous family with severe developmental delay, microcephaly, seizures, feeding difficulties, and osteopenia extends the phenotypic spectrum of autosomal recessive EXT2-related syndrome (AREXT2). European Journal of Medical Genetics, 62(4), 259. https://doi.org/10.1016/j.ejmg.2018.07.025

Chicago Style (17th ed.) Citation

El-Bazzal, Lara, Alexandre Atkinson, Anne-Celine Gillart, Marc Obeid, Valérie Delague, and André Mégarbané. "A Novel EXT2 Mutation in a Consanguineous Family with Severe Developmental Delay, Microcephaly, Seizures, Feeding Difficulties, and Osteopenia Extends the Phenotypic Spectrum of Autosomal Recessive EXT2-related Syndrome (AREXT2)." European Journal of Medical Genetics 62, no. 4 (2019): 259. https://doi.org/10.1016/j.ejmg.2018.07.025.

MLA (9th ed.) Citation

El-Bazzal, Lara, et al. "A Novel EXT2 Mutation in a Consanguineous Family with Severe Developmental Delay, Microcephaly, Seizures, Feeding Difficulties, and Osteopenia Extends the Phenotypic Spectrum of Autosomal Recessive EXT2-related Syndrome (AREXT2)." European Journal of Medical Genetics, vol. 62, no. 4, 2019, p. 259, https://doi.org/10.1016/j.ejmg.2018.07.025.