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Publication date
2017 Apr 06
Authors
Jansen, S Geuer, S Pfundt, R Brough, R Ghongane, P Herkert, JC Marco, EJ Willemsen, MH Kleefstra, T Hannibal, M Shieh, JT Lynch, SA Flinter, F FitzPatrick, DR Gardham, A Bernhard, B Ragge, N Newbury-Ecob, R Bernier, R Kvarnung, M Magnusson, EAH Wessels, MW van Slegtenhorst, MA Monaghan, KG de Vries, P Veltman, JA Lord, CJ Vissers, LELM de Vries, BBA
Group authors
Deciphering Dev Disorders Study
Author KI Usernames
Kvarnung, M|malkva
Pubmed ID
28343630
Journal
American journal of human genetics
Doctype
Article
KI Connection
Låg
Mesh SV
Barn Cellcykel Exoner Förskolebarn Intellektuell funktionsnedsättning Mutation Människa Proteinfosfatas 2C Unga vuxna Ungdomar
Mesh EN
Cell Cycle Exons Intellectual Disability Mutation Protein Phosphatase 2C
First date
2017-04-16T10:18:22.353Z