| Affiliation auteurs | !!!! Error affiliation !!!! |
| Titre | Integrated genome and transcriptome analyses solves about one third of the patients with rare developmental disorders and negative first-line molecular investigations |
| Type de publication | Journal Article |
| Year of Publication | 2020 |
| Auteurs | Vitobello A., F. Mau-Them T, Bruel A.L, Duffourd Y., Tisserant E., Callier P., Moutton S., Nambot S., Lehalle D., Jean-Marcais N., Delanne J., Racine C., Thevenon J., Poe C., Jouan T., Chevarin M., Willems M., Coubes C., Genevieve D., Houcinat N., Masurel-Paulet A., Mosca-Boidron A., Sorlin A., Isidor B., Heide S., Afenjar A., Rodriguez D., Mignot C., Heron D., Vincent M., Charles P., Odent S., Dubourg C., Faudet A., Keren B., Cogne B., Boland A., Olaso R., Philippe C., Deleuze J.F, Faivre L., Thauvin-Robinet C. |
| Journal | EUROPEAN JOURNAL OF HUMAN GENETICS |
| Volume | 28 |
| Pagination | 65-66 |
| Date Published | DEC |
| Type of Article | Meeting Abstract |
| ISSN | 1018-4813 |
