The analysis of parental origin of alleles may detect susceptibility loci for complex disorders

Human Heredity

Volumn 49, Issue 4, 1999, Pages 197-204

  Paterson, Andrew D ^a   Naimark, David M J ^b   Petronis, Arturas ^a,c  

^a UNIVERSITY OF TORONTO   (Canada)

^b SUNNYBROOK RESEARCH INSTITUTE   (Canada)

^c CENTRE FOR ADDICTION AND MENTAL HEALTH   (Canada)

Author keywords

Complex disorders; Genome scan; Genomic imprinting; Linkage analysis; Parent of origin; Type 1 diabetes

Indexed keywords

ALLELE; ARTICLE; CHROMOSOME 16Q; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC DISORDER; GENETIC SUSCEPTIBILITY; GENOME IMPRINTING; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; MAJOR CLINICAL STUDY; MOLECULAR CLONING; PARENT; SIBLING;

ALLELES; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 6; DIABETES MELLITUS, TYPE 1; FATHERS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOMIC IMPRINTING; GENOTYPE; HUMANS; LINKAGE (GENETICS); MALE; MOTHERS; PEDIGREE;

EID: 0032809054     PISSN: 00015652     EISSN: None     Source Type: Journal    
DOI: 10.1159/000022875     Document Type: Article

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