APA (7th ed.) Citation

Gebril OH, Cheong SS, Hardcastle AJ, Abdelraouf ER, Eid SR, & Elsaied M. (2017). Absence of CHRDL1 and FOXC1 sequence changes in two brothers with Megalocornea-Mental Retardation Syndrome. Journal of Neurology, Neurological Science and Disorders - Peertechz Publications. https://doi.org/10.17352/jnnsd.000017

Chicago Style (17th ed.) Citation

Gebril OH, Cheong SS, Hardcastle AJ, Abdelraouf ER, Eid SR, and Elsaied M. Absence of CHRDL1 and FOXC1 Sequence Changes in Two Brothers with Megalocornea-Mental Retardation Syndrome. Journal of Neurology, Neurological Science and Disorders - Peertechz Publications, 2017. https://doi.org/10.17352/jnnsd.000017.

MLA (9th ed.) Citation

Gebril OH, et al. Absence of CHRDL1 and FOXC1 Sequence Changes in Two Brothers with Megalocornea-Mental Retardation Syndrome. Journal of Neurology, Neurological Science and Disorders - Peertechz Publications, 2017. https://doi.org/10.17352/jnnsd.000017.