@article{vegas:hal-01920261,
TITLE = {Delineating FOXG1 syndrome},
AUTHOR = {Vegas, Nancy and Cavallin, Mara and Maillard, Camille and Boddaert, Nathalie and Toulouse, Joseph and Schaefer, Elise and Lerman-Sagie, Tally and Lev, Dorit and Magalie, Barth and Moutton, S{\'e}bastien and Haan, Eric and Isidor, Bertrand and H{\'e}ron, Delphine and Milh, Mathieu and Rondeau, St{\'e}phane and Michot, Caroline and Valence, Stephanie and Wagner, Sabrina and Hully, Marie and Mignot, Cyril and Masurel, Alice and Datta, Alexandre and Odent, Sylvie and Nizon, Mathilde and Lazaro, Leila and Vincent, Marie and Cogn{\'e},
Benjamin and Guerrot, Anne Marie and Arpin, St{\'e}phanie and Pedespan, Jean Michel and Caubel, Isabelle and Pontier, B{\'e}n{\'e}dicte and Troude, Baptiste and Rivier, Francois and Philippe, Christophe and Bienvenu, Thierry and Spitz, Marie-Aude and Bery, Amandine and Bahi-Buisson, Nadia},
URL = {https://hal.science/hal-01920261},
JOURNAL = {Neurology Genetics},
PUBLISHER = {American Academy of Neurology},
VOLUME = {4},
NUMBER = {6},
PAGES = {e281},
YEAR = {2018},
MONTH = Dec, DOI = {10.1212/NXG.0000000000000281},
PDF = {https://hal.science/hal-01920261/file/e281.full.pdf},
HAL_ID = {hal-01920261},
HAL_VERSION = {v1},
}
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