APA
Froyen G., Bauters M., Boyle J., Van Esch H., Govaerts K., van Bokhoven H., Ropers H., Moraine C., Chelly J., Fryns J., Marynen P., Gecz J. & Turner G. (20071010). Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region. : Human genetics.
Chicago
Froyen Guy, Bauters Marijke, Boyle Jackie, Van Esch Hilde, Govaerts Karen, van Bokhoven Hans, Ropers Hans-Hilger, Moraine Claude, Chelly Jamel, Fryns Jean-Pierre, Marynen Peter, Gecz Jozef and Turner Gillian. 20071010. Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region. : Human genetics.
Harvard
Froyen G., Bauters M., Boyle J., Van Esch H., Govaerts K., van Bokhoven H., Ropers H., Moraine C., Chelly J., Fryns J., Marynen P., Gecz J. and Turner G. (20071010). Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region. : Human genetics.
MLA
Froyen Guy, Bauters Marijke, Boyle Jackie, Van Esch Hilde, Govaerts Karen, van Bokhoven Hans, Ropers Hans-Hilger, Moraine Claude, Chelly Jamel, Fryns Jean-Pierre, Marynen Peter, Gecz Jozef and Turner Gillian. Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region. : Human genetics. 20071010.