about
Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability.TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mahshid S Azamian
@ast
Mahshid S Azamian
@en
Mahshid S Azamian
@es
Mahshid S Azamian
@nl
type
label
Mahshid S Azamian
@ast
Mahshid S Azamian
@en
Mahshid S Azamian
@es
Mahshid S Azamian
@nl
prefLabel
Mahshid S Azamian
@ast
Mahshid S Azamian
@en
Mahshid S Azamian
@es
Mahshid S Azamian
@nl
P106
P1153
56007257700
P31
P496
0000-0002-8543-8284