@article{cherot:hal-01743766,
TITLE = {Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients},
AUTHOR = {Ch{\'e}rot, E and Keren, B and Dubourg, C and Carr{\'e},
W and Fradin, M and Lavillaureix, A and Afenjar, A and Burglen, L and Whalen, S and Charles, P and Marey, I and Heide, S and Jacquette, A and Heron, D and Doummar, D and Rodriguez, D and Billette de Villemeur, T and Moutard, M-L and Gu{\"e}t, A and Xavier, J and P{\'e}risse, D and Cohen, David and Demurger, F and Qu{\'e}lin, C and Depienne, C and Odent, S and Nava, C and David, V and Pasquier, L and Mignot, C},
URL = {https://univ-rennes.hal.science/hal-01743766},
JOURNAL = {Clinical Genetics},
PUBLISHER = {Wiley},
VOLUME = {93},
NUMBER = {3},
PAGES = {567-576},
YEAR = {2018},
MONTH = Mar, DOI = {10.1111/cge.13102},
KEYWORDS = {medical exome ; molecular strategy ; intellectual disability ; autism},
PDF = {https://univ-rennes.hal.science/hal-01743766/file/Ch%C3%A9rot%20et%20al.%20-%20Using%20medical%20exome%20sequencing%20to%20identify%20the%20cau%20%281%29.pdf},
HAL_ID = {hal-01743766},
HAL_VERSION = {v1},
}