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Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome
Laffargue, F., Bourthoumieu, S., Llanas, B., Baudouin, V., Lahoche, A., Morin, D., Bessenay, L., De Parscau, L., Cloarec, S., Delrue, M.-A., Taupiac, E., Dizier, E., Laroche, C., Bahans, C., Yardin, CVolume:
100
Language:
english
Journal:
Archives of Disease in Childhood
DOI:
10.1136/archdischild-2014-306810
Date:
March, 2015
File:
PDF, 1.42 MB
english, 2015