Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders

Molecular Autism

Volumn 1, Issue 1, 2010, Pages

  Cannon, Dale ^a   Miller, Judith ^a   Robison, Reid ^a   Villalobos, Michele ^a   Wahmhoff, Natalie ^a   Allen Brady, Kristina ^a   McMahon, William ^a   Coon, Hilary ^a  

^a UNIVERSITY OF UTAH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTISM; CHILD; COMPUTER PROGRAM; DISEASE MARKER; DISEASE SEVERITY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC RISK; GENOME ANALYSIS; GENOTYPE; HERITABILITY; HUMAN; INSISTENCE OF SAMENESS; INTELLIGENCE QUOTIENT; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MONTE CARLO METHOD; PEDIGREE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; PROBABILITY; RATING SCALE; REPETITIVE SENSORY MOTOR ACTION; RISK ASSESSMENT; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; UNITED STATES;

EID: 77956352770     PISSN: None     EISSN: 20402392     Source Type: Journal    
DOI: 10.1186/2040-2392-1-3     Document Type: Article

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