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

Psychiatric Genetics

Volumn 22, Issue 5, 2012, Pages 226-234

  Peter, Beate ^a   Matsushita, Mark ^a   Raskind, Wendy H ^a,b  

^a UNIVERSITY OF WASHINGTON   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

6p21; 7q32; 7q36; 8q24; genome wide linkage analysis; multigenerational family; sequential motor speech task; speech sound disorder

Indexed keywords

MICROSATELLITE DNA;

ADOLESCENT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DYSLEXIA; ENDOPHENOTYPE; FAMILIAL DISEASE; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC ASSOCIATION; GENETIC TRAIT; HUMAN; LANGUAGE DISABILITY; LINKAGE ANALYSIS; MALE; MOTOR DYSFUNCTION; NONPARAMETRIC TEST; PARAMETRIC TEST; PILOT STUDY; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SPEECH DEVELOPMENT; SPEECH DISORDER; SPEECH SOUND DISORDER;

CHILD; CHILD, PRESCHOOL; ENDOPHENOTYPES; FAMILY CHARACTERISTICS; FEMALE; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; LANGUAGE DISORDERS; LOD SCORE; MALE; PEDIGREE;

EID: 84866058422     PISSN: 09558829     EISSN: 14735873     Source Type: Journal    
DOI: 10.1097/YPG.0b013e328353ae92     Document Type: Article

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