FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum.
about
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.Prospective investigation of FOXP1 syndrome.Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders.Haploinsufficiency of NR4A2 is associated with a neurodevelopmental phenotype with prominent language impairment.Mapping of Human FOXP2 Enhancers Reveals Complex Regulation.BCL11A frameshift mutation associated with dyspraxia and hypotonia affecting the fine, gross, oral, and speech motor systems.Saliva samples as a source of DNA for high throughput genotyping: an acceptable and sufficient means in improvement of risk estimation throughout mammographic diagnostics.Interstitial deletion within 7q31.1q31.3 in a woman with mild intellectual disability and schizophrenia.What aDNA can (and cannot) tell us about the emergence of language and speech
P2860
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P2860
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
FOXP2 variants in 14 individua ...... ational and clinical spectrum.
@en
FOXP2 variants in 14 individua ...... ational and clinical spectrum.
@nl
type
label
FOXP2 variants in 14 individua ...... ational and clinical spectrum.
@en
FOXP2 variants in 14 individua ...... ational and clinical spectrum.
@nl
prefLabel
FOXP2 variants in 14 individua ...... ational and clinical spectrum.
@en
FOXP2 variants in 14 individua ...... ational and clinical spectrum.
@nl
P2093
P2860
P50
P1476
FOXP2 variants in 14 individua ...... ational and clinical spectrum.
@en
P2093
Angelika Riess
Dieter Gläser
Harald Rabe
Jürgen Kohlhase
Kate E Chandler
Katharina Steindl
Mandy Krumbiegel
Miriam S Reuter
Miriam Stampfer
P2860
P356
10.1136/JMEDGENET-2016-104094
P407
P577
2016-08-29T00:00:00Z