Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.

Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.

Item
http://www.wikidata.org/entity/Q36125741
Direct and octave-shifted pitch matching during nonword imitations in men, women, and childrenNonspeech Oral Movements and Oral Motor Disorders: A Narrative ReviewAssociations among measures of sequential processing in motor and linguistics tasks in adults with and without a family history of childhood apraxia of speech: a replication study.Genetic insights into the functional elements of language.The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domainsGenetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.Linkage analysis in a Dutch population isolate shows no major gene for left-handedness or atypical language lateralizationLanguage Impairment Resulting from a de novo Deletion of 7q32.1q33.Deficits 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.A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker.Genome-Wide Studies of Specific Language Impairment.Sequential processing deficit as a shared persisting biomarker in dyslexia and childhood apraxia of speech.Two unrelated children with overlapping 6q25.3 deletions, motor speech disorders, and language delays.
P2860

Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family.

Item
http://www.wikidata.org/entity/Q36125741
description
2012 nî lūn-bûn
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