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Details on Person Diagnostic exome sequencing in persons with severe intellectual disability

Class:Id	LiteratureReference:9618944
_displayName	Diagnostic exome sequencing in persons with severe intellectual disability
_timestamp	2018-09-13 15:40:19
author	[Person:5661062] de Ligt, Joep [Person:5661020] Willemsen, Marjolein H [Person:5661067] van Bon, Bregje W M [Person:5661071] Kleefstra, Tjitske [Person:548689] Yntema, HG [Person:9618940] Kroes, Thessa [Person:5661068] Vulto-van Silfhout, Anneke T [Person:9618936] Koolen, David A [Person:5678453] de Vries, Petra [Person:4549377] Gilissen, Christian [Person:5661052] del Rosario, Marisol [Person:4549395] Hoischen, Alexander [Person:3274533] Scheffer, Hans [Person:5661031] de Vries, Bert B A [Person:3247887] Brunner, Han G [Person:2466819] Veltman, Joris A [Person:5661046] Vissers, Lisenka E L M
created	[InstanceEdit:9618943] Orlic-Milacic, Marija, 2018-09-13
journal	N. Engl. J. Med.
pages	1921-9
pubMedIdentifier	23033978
title	Diagnostic exome sequencing in persons with severe intellectual disability
volume	367
year	2012
(literatureReference)	[Pathway:9618928] Autosomal dominant non-syndromic intellectual disability due to defects in CAMK2G [Homo sapiens]
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No pathways have been reviewed or authored by Diagnostic exome sequencing in persons with severe intellectual disability (9618944)