AMMECR1 : a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis.

MLA

Andreoletti, Gaia, et al. “AMMECR1 : A Single Point Mutation Causes Developmental Delay, Midface Hypoplasia and Elliptocytosis.” Journal of Medical Genetics, vol. 54, no. 4, Apr. 2017, pp. 269–77. EBSCOhost, https://doi.org/10.1136/jmedgenet-2016-104100.

APA

Andreoletti, G., Seaby, E. G., Dewing, J. M., O’Kelly, I., Lachlan, K., Gilbert, R. D., & Ennis, S. (2017). AMMECR1 : a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis. Journal of Medical Genetics, 54(4), 269–277. https://doi.org/10.1136/jmedgenet-2016-104100

Chicago

Andreoletti, Gaia, Eleanor G Seaby, Jennifer M Dewing, Ita O’Kelly, Katherine Lachlan, Rodney D Gilbert, and Sarah Ennis. 2017. “AMMECR1 : A Single Point Mutation Causes Developmental Delay, Midface Hypoplasia and Elliptocytosis.” Journal of Medical Genetics 54 (4): 269–77. doi:10.1136/jmedgenet-2016-104100.