about
Refining analyses of copy number variation identifies specific genes associated with developmental delayVariation in a range of mTOR-related genes associates with intracranial volume and intellectual disability.Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder.Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome
P50
description
Forscher
@de
chercheur
@fr
investigador
@es
researcher
@en
ricercatore
@it
wetenschapper
@nl
研究者
@zh
name
Reijnders MRF
@ast
Reijnders MRF
@en
Reijnders MRF
@es
Reijnders MRF
@nl
type
label
Reijnders MRF
@ast
Reijnders MRF
@en
Reijnders MRF
@es
Reijnders MRF
@nl
prefLabel
Reijnders MRF
@ast
Reijnders MRF
@en
Reijnders MRF
@es
Reijnders MRF
@nl
P106
P31
P496
0000-0002-6379-7147