Cite

    Laffargue, F., Bourthoumieu, S., Llanas, B., Baudouin, V., Lahoche, A., Morin, D., Bessenay, L., De Parscau, L., Cloarec, S., Delrue, M., Taupiac, E., Dizier, E., Laroche, C., Bahans, C., Yardin, C., Lacombe, D., & Guigonis, V. (2015). towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. Archives of disease in childhood, 100(3), 259–264. http://access.bl.uk/ark:/81055/vdc_100135549050.0x00005a