| Affiliation auteurs | !!!! Error affiliation !!!! |
| Titre | Genotype and phenotype features of 22 patients with intellectual disability caused by MED13L variations |
| Type de publication | Journal Article |
| Year of Publication | 2018 |
| Auteurs | Smol T., Petit F., Gerard B., Keren B., Thuillier C., Sanlavile D., Boudry-Labis E., Lesca G., Heron D., Faivre L., Nava C., Kuentz P., Devillard F., Saugier-Veber P., Guerrot A., Verloes A., Coubes C., Caumes R., Dieux-Coeslier A., Boute-Benejean O., Bouquillon S., Afenjar A., Field M., Zarate Y.A, Marey I., Lapi E., Fassi E., Couton C., Roscioli T., Doco-Fenzy M., Porchet N., Roche-Lestienne C., Manouvrier-Hanu S., Piton A., Ghoumid J. |
| Journal | EUROPEAN JOURNAL OF HUMAN GENETICS |
| Volume | 26 |
| Pagination | 347-348 |
| Date Published | OCT |
| Type of Article | Meeting Abstract |
| ISSN | 1018-4813 |
