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Publication date
2017 Apr
Authors
Stessman, HAF Xiong, B Coe, BP Wang, TY Hoekzema, K Fenckova, M Kvarnung, M Gerdts, J Trinh, S Cosemans, N Vives, L Lin, J Turner, TN Santen, G Ruivenkamp, C Kriek, M van Haeringen, A Aten, E Friend, K Liebelt, J Barnett, C Haan, E Shaw, M Gecz, J Anderlid, BM Nordgren, A Lindstrand, A Schwartz, C Kooy, RF Vandeweyer, G Helsmoortel, C Romano, C Alberti, A Vinci, M Avola, E Giusto, S Courchesne, E Pramparo, T Pierce, K Nalabolu, S Amaral, DG Scheffer, IE Delatycki, MB Lockhart, PJ Hormozdiari, F Harich, B Castells-Nobau, A Xia, K Peeters, H Nordenskjold, M Schenck, A Bernier, RA Eichler, EE
Author KI Usernames
Anderlid, BM|briand Kvarnung, M|malkva Lindstrand, A|alindst Nordenskjold, M|magnor Nordenskjöld, M|magnor Nordgren, A|annord
Pubmed ID
28191889
Journal
Nature genetics
Doctype
Article
KI Connection
Medel
Mesh SV
Autism Fenotyp Intellektuell funktionsnedsättning Kvinnlig Manlig Mutation Människa Utvecklingsstörningar
Mesh EN
Autistic Disorder Developmental Disabilities Intellectual Disability Mutation Phenotype
First date
2017-04-09T11:22:19.843Z