Monogenic and chromosomal causes of isolated speech and language impairment.
about
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker.Haploinsufficiency of NR4A2 is associated with a neurodevelopmental phenotype with prominent language impairment.BCL11A frameshift mutation associated with dyspraxia and hypotonia affecting the fine, gross, oral, and speech motor systems.Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations.
P2860
Monogenic and chromosomal causes of isolated speech and language impairment.
description
2015 nî lūn-bûn
@nan
2015 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Monogenic and chromosomal causes of isolated speech and language impairment.
@ast
Monogenic and chromosomal causes of isolated speech and language impairment.
@en
Monogenic and chromosomal causes of isolated speech and language impairment.
@nl
type
label
Monogenic and chromosomal causes of isolated speech and language impairment.
@ast
Monogenic and chromosomal causes of isolated speech and language impairment.
@en
Monogenic and chromosomal causes of isolated speech and language impairment.
@nl
prefLabel
Monogenic and chromosomal causes of isolated speech and language impairment.
@ast
Monogenic and chromosomal causes of isolated speech and language impairment.
@en
Monogenic and chromosomal causes of isolated speech and language impairment.
@nl
P2860
P1476
Monogenic and chromosomal causes of isolated speech and language impairment.
@en
P2093
B W M van Bon
C P Barnett
P2860
P304
P356
10.1136/JMEDGENET-2015-103161
P407
P577
2015-07-02T00:00:00Z