Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
| Author | dc.contributor.author | Davies, RW | |
| Author | dc.contributor.author | Fiksinski, AM | |
| Author | dc.contributor.author | Breetvelt, EJ | |
| Author | dc.contributor.author | Williams, NM | |
| Author | dc.contributor.author | Hooper, SR | |
| Author | dc.contributor.author | Monfeuga, T | |
| Author | dc.contributor.author | Bassett, AS | |
| Author | dc.contributor.author | Owen, MJ | |
| Author | dc.contributor.author | Gur, RE | |
| Author | dc.contributor.author | Morrow, BE | |
| Author | dc.contributor.author | McDonald-McGinn, DM | |
| Author | dc.contributor.author | Swillen, A | |
| Author | dc.contributor.author | Chow, EWC | |
| Author | dc.contributor.author | van den Bree, M | |
| Author | dc.contributor.author | Emanuel, BS | |
| Author | dc.contributor.author | Vermeesch, JR | |
| Author | dc.contributor.author | van Amelsvoort, T | |
| Author | dc.contributor.author | Arango, C | |
| Author | dc.contributor.author | Armando, M | |
| Author | dc.contributor.author | Campbell, LE | |
| Author | dc.contributor.author | Cubells, JF | |
| Author | dc.contributor.author | Eliez, S | |
| Author | dc.contributor.author | Garcia-Minaur, S | |
| Author | dc.contributor.author | Gothelf, D | |
| Author | dc.contributor.author | Kates, WR | |
| Author | dc.contributor.author | Murphy, KC | |
| Author | dc.contributor.author | Murphy, CM | |
| Author | dc.contributor.author | Murphy, DG | |
| Author | dc.contributor.author | Philip, N | |
| Author | dc.contributor.author | Repetto, GM | |
| Author | dc.contributor.author | Shashi, V | |
| Author | dc.contributor.author | Simon, TJ | |
| Author | dc.contributor.author | Suner, DH | |
| Author | dc.contributor.author | Vicari, S | |
| Author | dc.contributor.author | Scherer, SW | |
| Author | dc.contributor.author | Bearden, CE | |
| Author | dc.contributor.author | Vorstman, JAS | |
| Admission date | dc.date.accessioned | 2022-12-27T13:58:56Z | |
| Available date | dc.date.available | 2022-12-27T13:58:56Z | |
| Publication date | dc.date.issued | 2020 | |
| Identifier | dc.identifier.issn | 1546170X | |
| Identifier | dc.identifier.issn | 10788956 | |
| Identifier | dc.identifier.other | 10.1038/s41591-020-1103-1 | |
| Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/190546 | |
| Lenguage | dc.language.iso | en | |
| Publisher | dc.publisher | Nature Research | |
| 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 | Nature Medicine | |
| Título | dc.title | Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome | |
| 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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