Genetic mapping in human disease

Science

Volumn 322, Issue 5903, 2008, Pages 881-888

  Altshuler, David ^a,b,c   Daly, Mark J ^a,b,c   Lander, Eric S ^a,c,d,e  

^a BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^b MASSACHUSETTS GENERAL HOSPITAL   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

^d MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^e WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DISEASE; EPIDEMIOLOGY; GENE EXPRESSION; GENOME; HERITABILITY; HOMINID;

DNA SEQUENCE; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC RISK; GENOME; GENOTYPE; HUMAN; INHERITANCE; PRIORITY JOURNAL; REVIEW; SYSTEMIC DISEASE;

CHROMOSOME MAPPING; CLONING, MOLECULAR; DISEASE; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; LINKAGE (GENETICS); LINKAGE DISEQUILIBRIUM; MUTATION; PHYSICAL CHROMOSOME MAPPING; POLYMORPHISM, SINGLE NUCLEOTIDE; QUANTITATIVE TRAIT, HERITABLE; RISK FACTORS; SELECTION (GENETICS);

EID: 55449120805     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1156409     Document Type: Review

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