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スタイル(17版)引用形式Gebril OH, Cheong SS, Hardcastle AJ, Abdelraouf ER, Eid SR, , 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(9版)引用形式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.