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Volumn 9, Issue 5, 2001, Pages 328-334
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Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21
a a a a a b c d e f a a |
Author keywords
Chromosome mapping; Genetic predisposition to disease; Inflammatory bowel diseases; Linkage; Lod score; Microsatellite repeats
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Indexed keywords
CHEMOKINE RECEPTOR CCR5;
INTERLEUKIN 4 RECEPTOR;
ADOLESCENT;
ADULT;
AGED;
ALLELE;
ARTICLE;
CHILD;
CHROMOSOME 1;
CHROMOSOME 12;
CHROMOSOME 14;
CHROMOSOME 16;
CHROMOSOME 3P;
CHROMOSOME 7;
CLINICAL FEATURE;
CONTROLLED STUDY;
CORRELATION FUNCTION;
CROHN DISEASE;
DISEASE PREDISPOSITION;
ENTERITIS;
FAMILY;
FEMALE;
FINLAND;
GENE DELETION;
GENE LOCUS;
GENETIC ANALYSIS;
GENETIC LINKAGE;
GENETIC SUSCEPTIBILITY;
HOMOZYGOSITY;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
PHENOTYPE;
POPULATION;
PRIORITY JOURNAL;
RISK ASSESSMENT;
SCORING SYSTEM;
ULCERATIVE COLITIS;
ALLELES;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 16;
CHROMOSOMES, HUMAN, PAIR 3;
FEMALE;
FINLAND;
GENETIC PREDISPOSITION TO DISEASE;
GENETIC SCREENING;
HUMANS;
INFLAMMATORY BOWEL DISEASES;
LINKAGE (GENETICS);
MALE;
MICROSATELLITE REPEATS;
MIDDLE AGED;
RECEPTORS, CCR5;
RECEPTORS, INTERLEUKIN-4;
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EID: 0034985821
PISSN: 10184813
EISSN: None
Source Type: Journal
DOI: 10.1038/sj.ejhg.5200626 Document Type: Article |
Times cited : (41)
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References (33)
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