@article{vitobello:cea-04419438,
TITLE = {Integrated genome and transcriptome analyses solves about one third of the patients with rare developmental disorders and negative first-line molecular investigations},
AUTHOR = {Vitobello, A. and Mau-Them, F. T. and Bruel, A. L. and Duffourd, Y. and Tisserant, E. and Callier, P. and Moutton, S. and Nambot, S. and Lehalle, D. and Jean-Marcais, N. and Delanne, J. and Racine, C. and Thevenon, J. and Poe, C. and Jouan, T. and Chevarin, M. and Willems, M. and Coubes, C. and Genevieve, D. and Houcinat, N. and Masurel-Paulet, A. and Mosca-Boidron, A. and Sorlin, A. and Isidor, B. and Heide, S. and Afenjar, A. and Rodriguez, D. and Mignot, C. and Heron, D. and Vincent, M. and Charles, P. and Odent, S. and Dubourg, C. and Faudet, A. and Keren, B. and Cogne, B. and Boland, Anne and Olaso, Robert and Philippe, C. and Deleuze, Jean-Fran{\c c}ois and Faivre, L. and Thauvin-Robinet, C.},
URL = {https://cea.hal.science/cea-04419438},
JOURNAL = {European Journal of Human Genetics},
PUBLISHER = {Nature Publishing Group},
VOLUME = {28},
NUMBER = {Suppl 1},
PAGES = {65-66},
YEAR = {2020},
HAL_ID = {cea-04419438},
HAL_VERSION = {v1},
}