HGV2011: Personalized genomic medicine meets the incidentalome

Human Mutation

Volumn 33, Issue 3, 2012, Pages 582-585

  Wilson Sayres, Melissa A ^a   Brookes, Anthony J ^b   Chanock, Stephen J ^c   Cheung, Vivian G ^d   Goldstein, David B ^e   Jin, Li ^f   Kwok, Pui Yan ^g,h  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF LEICESTER   (United Kingdom)

^c NATIONAL CANCER INSTITUTE   (United States)

^d UNIVERSITY OF PENNSYLVANIA   (United States)

^e HOSPITAL FOR SICK CHILDREN   (Canada)

^f FUDAN UNIVERSITY   (China)

^g UNIVERSITY OF CALIFORNIA   (United States)

^h NONE   (United States)

Author keywords

GWAS; Human variation; Medical genomics; SNP

Indexed keywords

BIOINFORMATICS; BODY MASS; CANCER SURVIVAL; CONFERENCE PAPER; COPY NUMBER VARIATION; DNA SEQUENCE; GENE FREQUENCY; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC COUNSELING; GENETIC VARIABILITY; GENOMICS; GENOTYPE; HEALTH CARE; HUMAN; HUMAN GENOME; MEDICAL RESEARCH; PERSONALIZED MEDICINE; POPULATION GENETICS; PRIORITY JOURNAL; RNA SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84857059712     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22008     Document Type: Conference Paper

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