Identification of rare variants from exome sequence in a large pedigree with autism

Human Heredity

Volumn 74, Issue 3-4, 2012, Pages 153-164

  Marchani, E E ^a   Chapman, N H ^a   Cheung, C Y K ^b   Ankenman, K ^b   Stanaway, I B ^b   Coon, H H ^c   Nickerson, D ^b   Bernier, R ^b   Brkanac, Z ^b   Wijsman, E M ^a,b  

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

^b UNIVERSITY OF WASHINGTON   (United States)

^c UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

Haplotype; Imputation; Inheritance vector; Linkage analysis; MCMC

Indexed keywords

ALLELE; ARTICLE; AUTISM; CHROMOSOME; CLINICAL ARTICLE; EXOME; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; INHERITANCE; MULTILOCUS SEQUENCE TYPING; PEDIGREE; RISK ASSESSMENT; SEQUENCE ANALYSIS;

EID: 84876459502     PISSN: 00015652     EISSN: 14230062     Source Type: Journal    
DOI: 10.1159/000346560     Document Type: Article

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