| Title: |
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome |
| Authors: |
Davies, RW; Fiksinski, AM; Breetvelt, EJ; Williams, NM; Hooper, SR; Monfeuga, T; Bassett, AS; Owen, MJ; Gur, RE; Morrow, BE; McDonald-McGinn, DM; Swillen, A; Chow, EWC; van den Bree, M; Emanuel, BS; Vermeesch, JR; van Amelsvoort, T; Arango, C; Armando, M; Campbell, LE; Cubells, JF; Eliez, S; Garcia-Minaur, S; Gothelf, D; Kates, WR; Murphy, KC; Murphy, CM; Murphy, DG; Philip, N; Repetto, GM; Shashi, V; Simon, TJ; Suner, DH; Vicari, S; Scherer, SW; Bearden, CE; Vorstman, JAS |
| Source: |
Nature Medicine |
| Publisher Information: |
Nature Research |
| Publication Year: |
2020 |
| Collection: |
Universidad de Chile: Repositorio académico |
| Document Type: |
article in journal/newspaper |
| File Description: |
application/pdf |
| Language: |
English |
| ISSN: |
1546170X; 10788956 |
| Relation: |
https://repositorio.uchile.cl/handle/2250/190546 |
| DOI: |
10.1038/s41591-020-1103-1 |
| Availability: |
https://doi.org/10.1038/s41591-020-1103-1; https://repositorio.uchile.cl/handle/2250/190546 |
| Rights: |
Attribution-NonCommercial-NoDerivs 3.0 Chile ; http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ |
| Accession Number: |
edsbas.BE5D314B |
| Database: |
BASE |