Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.
about
Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.Accelerated FoxP2 evolution in echolocating batsWhole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.Intervention for childhood apraxia of speechA functional genetic link between distinct developmental language disordersChildhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.The archaeological record speaks: bridging anthropology and linguisticsGenetic advances in the study of speech and language disordersThe distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disordersHigh-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disordersAssessing the impact of FOXP1 mutations on developmental verbal dyspraxiaSinging mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and languageAbsence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaKnockout of Foxp2 disrupts vocal development in mice.Generation of mice with a conditional Foxp2 null alleleRecent Advances in the Genetics of Vocal LearningAssociation study of stuttering candidate genes GNPTAB, GNPTG and NAGPA with dyslexia in Chinese population.Globularity and language-readiness: generating new predictions by expanding the set of genes of interestStuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese populationCNTNAP2 and language processing in healthy individuals as measured with ERPsRecent advances in the genetics of language impairmentDomain-specific regulation of foxP2 CNS expression by lef1Central timing deficits in subtypes of primary speech disorders.Data-driven subclassification of speech sound disorders in preschool children.Linking neurogenetics and individual differences in language learning: the dopamine hypothesis.Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridizationComputational prosodic markers for autism.Encoding, memory, and transcoding deficits in Childhood Apraxia of Speech.The hypothesis of apraxia of speech in children with autism spectrum disorder.Prevalence and phenotype of childhood apraxia of speech in youth with galactosemia.Automated Assessment of Prosody Production.A nonword repetition task for speakers with misarticulations: the Syllable Repetition Task (SRT)Conservation and diversity of Foxp2 expression in muroid rodents: functional implications.12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech.Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders.Retinoic Acid Signaling: A New Piece in the Spoken Language Puzzle.The Genetic Basis of Thought Disorder and Language and Communication Disturbances in Schizophrenia.Rearrangements of the Williams-Beuren syndrome locus: molecular basis and implications for speech and language development.Genetic insights into the functional elements of language.Zebrafish foxP2 zinc finger nuclease mutant has normal axon pathfinding.
P2860
Q21092748-38AFBD65-7246-4A48-9056-E4ADF03B3303Q21144431-4BF072B7-1356-43A7-AA5E-7FB9C27EF695Q21198726-A6109D03-8F67-47A0-A238-A46450042FE3Q24242172-B423309E-0736-4696-A348-5FFF4C7C0A7DQ24312638-7DB496CA-3DBD-418D-BFBF-9C40695D7403Q24604419-E94254BE-849E-4C8A-B664-726D92904BC9Q24604714-B410AB4D-4E3C-44E5-8506-E6AFB0CD32E2Q24609855-1B48F58C-1ED8-4AC7-99D4-6C782A40881DQ24629522-15EED868-7AF0-4B06-9CE3-582990C69094Q24648773-2EDDB473-FD76-4C4F-AFAB-FDD227A32353Q24649522-BDF5E4C6-4E3F-4598-BDBE-BE19BC58D264Q24658435-899A0E1A-5C52-4E31-80CE-23DC1A969CB6Q24672211-CB063993-A639-4BAA-AB15-8FE46D836A67Q27330219-6988AF23-462A-45FA-9D30-510194E20CDFQ28586785-519F1134-EF73-4246-A9AA-CCB6FA6B98ABQ28645740-0D9915F7-52C5-4AD0-86F7-360FEB6067DDQ28649364-A07A4A07-4E09-4259-9431-A2A4D5C5C19BQ28651479-1D017FDF-4CE9-42FD-A7A0-E9F555791C74Q28651994-3F09AF7C-FEDE-4322-97F5-7DB75C5D1520Q28714875-D2780624-8588-4AE8-9635-F8565B67AD69Q28748712-5AB480D0-0FA8-4805-9260-30025D6DF5ABQ28756604-04B5A546-2DB5-4651-ABD3-18333681B943Q30367983-308A245F-E012-4222-BAAA-9D3B4777E781Q30417794-314A9C08-93D4-4206-A6DD-240C5035FD39Q30441297-6062F8C8-FA40-4DF7-A46F-2D31D21D2EADQ30447724-2D6E9FFC-BBA0-45D6-8A10-641A325D1913Q30449594-6866FD9A-6853-4300-9CBB-34A2461B6724Q30457923-4C65A9BE-C028-4328-A84C-7A0DE233F594Q30469038-D2FF8C1B-5949-4865-B45C-A81011DC54FCQ30469080-91D333EC-5C9B-480E-86EE-10B35851FE90Q30478993-755C8F46-FFBA-491A-8BE2-4177C5B264F8Q30479393-7980960A-502D-41AE-BCA8-550DFBBCBB9FQ30484346-767B447C-B346-4576-90BF-559B1F26FC88Q30529890-CB51D135-D727-48D7-8BA1-497E76012B27Q30823070-806579FA-22ED-4026-946B-5B7A1F7FFD3FQ33362024-B38CCA66-BA0E-40C8-8B04-E1F352834823Q33649758-577E031A-201A-4DA3-9B94-84A1D54DA6F2Q33945408-93B33C23-28D8-45A9-B6F9-6B01A6D6435FQ34349576-57065900-94C7-484D-9542-AFBC1D469DADQ34399614-09F0B303-D0BF-40FD-AE0A-DCACB8F6CD43
P2860
Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Speech, prosody, and voice cha ...... translocation affecting FOXP2.
@ast
Speech, prosody, and voice cha ...... translocation affecting FOXP2.
@en
Speech, prosody, and voice cha ...... translocation affecting FOXP2.
@nl
type
label
Speech, prosody, and voice cha ...... translocation affecting FOXP2.
@ast
Speech, prosody, and voice cha ...... translocation affecting FOXP2.
@en
Speech, prosody, and voice cha ...... translocation affecting FOXP2.
@nl
prefLabel
Speech, prosody, and voice cha ...... translocation affecting FOXP2.
@ast
Speech, prosody, and voice cha ...... translocation affecting FOXP2.
@en
Speech, prosody, and voice cha ...... translocation affecting FOXP2.
@nl
P2093
P356
P1476
Speech, prosody, and voice cha ...... translocation affecting FOXP2.
@en
P2093
Charles A Williams
J Bruce Tomblin
Joseph R Duffy
Katharine H Odell
Lawrence D Shriberg
P304
P356
10.1044/1092-4388(2006/038)
P577
2006-06-01T00:00:00Z