dc.creator | Cuvertino, S | |
dc.creator | Hartill, V | |
dc.creator | Colyer, A | |
dc.creator | Garner, T | |
dc.creator | Nair, N | |
dc.creator | Al-Gazali, L | |
dc.creator | Canham, N | |
dc.creator | Faundes, V | |
dc.creator | Flinter, F | |
dc.creator | Hertecant, J | |
dc.creator | Holder-Espinasse, M | |
dc.creator | Jackson, B | |
dc.creator | Lynch, SA | |
dc.creator | Nadat, F | |
dc.creator | Narasimhan, VM | |
dc.creator | Peckham, M | |
dc.creator | Sellers, R | |
dc.creator | Seri, M | |
dc.creator | Montanari, F | |
dc.creator | Southgate, L | |
dc.creator | Squeo, GM | |
dc.creator | Trembath, R | |
dc.creator | van Heel, D | |
dc.creator | Venuto, S | |
dc.creator | Weisberg, D | |
dc.creator | Stals, K | |
dc.creator | Ellard, S | |
dc.creator | Barton, A | |
dc.creator | Kimber, SJ | |
dc.creator | Sheridan, E | |
dc.creator | Merla, G | |
dc.creator | Stevens, A | |
dc.creator | Johnson, CA | |
dc.creator | Banka, S | |
dc.date.accessioned | 2022-12-27T14:05:12Z | |
dc.date.accessioned | 2023-05-18T20:23:38Z | |
dc.date.available | 2022-12-27T14:05:12Z | |
dc.date.available | 2023-05-18T20:23:38Z | |
dc.date.created | 2022-12-27T14:05:12Z | |
dc.date.issued | 2020 | |
dc.identifier | 15300366 | |
dc.identifier | 10983600 | |
dc.identifier | 10.1038/s41436-020-0784-7 | |
dc.identifier | https://repositorio.uchile.cl/handle/2250/190859 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/6295824 | |
dc.language | en | |
dc.publisher | Springer Nature | |
dc.rights | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Chile | |
dc.source | Genetics in Medicine | |
dc.title | Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3) | |
dc.type | Artículo de revista | |