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)
| Author | dc.contributor.author | Cuvertino, S | |
| Author | dc.contributor.author | Hartill, V | |
| Author | dc.contributor.author | Colyer, A | |
| Author | dc.contributor.author | Garner, T | |
| Author | dc.contributor.author | Nair, N | |
| Author | dc.contributor.author | Al-Gazali, L | |
| Author | dc.contributor.author | Canham, N | |
| Author | dc.contributor.author | Faundes, V | |
| Author | dc.contributor.author | Flinter, F | |
| Author | dc.contributor.author | Hertecant, J | |
| Author | dc.contributor.author | Holder-Espinasse, M | |
| Author | dc.contributor.author | Jackson, B | |
| Author | dc.contributor.author | Lynch, SA | |
| Author | dc.contributor.author | Nadat, F | |
| Author | dc.contributor.author | Narasimhan, VM | |
| Author | dc.contributor.author | Peckham, M | |
| Author | dc.contributor.author | Sellers, R | |
| Author | dc.contributor.author | Seri, M | |
| Author | dc.contributor.author | Montanari, F | |
| Author | dc.contributor.author | Southgate, L | |
| Author | dc.contributor.author | Squeo, GM | |
| Author | dc.contributor.author | Trembath, R | |
| Author | dc.contributor.author | van Heel, D | |
| Author | dc.contributor.author | Venuto, S | |
| Author | dc.contributor.author | Weisberg, D | |
| Author | dc.contributor.author | Stals, K | |
| Author | dc.contributor.author | Ellard, S | |
| Author | dc.contributor.author | Barton, A | |
| Author | dc.contributor.author | Kimber, SJ | |
| Author | dc.contributor.author | Sheridan, E | |
| Author | dc.contributor.author | Merla, G | |
| Author | dc.contributor.author | Stevens, A | |
| Author | dc.contributor.author | Johnson, CA | |
| Author | dc.contributor.author | Banka, S | |
| Admission date | dc.date.accessioned | 2022-12-27T14:05:12Z | |
| Available date | dc.date.available | 2022-12-27T14:05:12Z | |
| Publication date | dc.date.issued | 2020 | |
| Identifier | dc.identifier.issn | 15300366 | |
| Identifier | dc.identifier.issn | 10983600 | |
| Identifier | dc.identifier.other | 10.1038/s41436-020-0784-7 | |
| Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/190859 | |
| Lenguage | dc.language.iso | en | |
| Publisher | dc.publisher | Springer Nature | |
| Type of license | dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Chile | |
| Link to License | dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
| Source | dc.source | Genetics in Medicine | |
| Título | 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) | |
| Document type | dc.type | Artículo de revista | |
| Cataloguer | uchile.catalogador | SCOPUS | |
| Indexation | uchile.index | Artículo de publicación ISI | |
| Indexation | uchile.index | Artículo de publicación SCOPUS | |
| Indexation | uchile.index | Artículo de publicación SCIELO | |
| uchile.cosecha | uchile.cosecha | SI |
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