Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
about
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorderNeurogenomics of speech and language disorders: the road aheadInvestigating the effects of copy number variants on reading and language performance.Recent Advances in the Genetics of Vocal Learning16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions.16p11.2 Deletion mice display cognitive deficits in touchscreen learning and novelty recognition tasksA highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.Monogenic and chromosomal causes of isolated speech and language impairment.Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.Genome-wide analysis identifies a role for common copy number variants in specific language impairmentDeficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech.Insights into the genetic foundations of human communication.New genes for focal epilepsies with speech and language disorders.Cognitive, Linguistic, and Motor Abilities in a Multigenerational Family with Childhood Apraxia of Speech.A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker.The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population.Late breaking chromosomes.Genome-Wide Studies of Specific Language Impairment.Focal Cortical Anomalies and Language Impairment in 16p11.2 Deletion and Duplication Syndrome.Two unrelated children with overlapping 6q25.3 deletions, motor speech disorders, and language delays.Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations.
P2860
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P2860
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
description
2012 nî lūn-bûn
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2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome
@nl
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
@ast
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
@en
type
label
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome
@nl
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
@ast
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
@en
prefLabel
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome
@nl
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
@ast
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
@en
P2093
P2860
P3181
P356
P1476
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
@en
P2093
Becky S Baas
Craig A Jackson
Edythe A Strand
Gordana Raca
Jennifer J Laffin
Kathy J Jakielski
Lawrence D Shriberg
Salman Kirmani
P2860
P2888
P304
P3181
P356
10.1038/EJHG.2012.165
P407
P577
2012-08-22T00:00:00Z
P5875
P6179
1008540139