Phenomics and the interpretation of personal genomes

Science Translational Medicine

Volumn 6, Issue 254, 2014, Pages

  Petrovski, Slavé ^a,b   Goldstein, David B ^a  

^a DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

BIOINFORMATICS; CLIENT SERVER APPLICATION; COMPUTER PROGRAM; EPILEPSY; EXOME; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME; GENOMICS; HUMAN; KCNT1 GENE; LACRIMAL GLAND DISEASE; NGLY1 GENE; NOTE; PHENOMICS; PHENOTYPE; SEIZURE; HUMAN GENOME; PERSONALIZED MEDICINE;

GENOME, HUMAN; HUMANS; INDIVIDUALIZED MEDICINE; PHENOTYPE;

EID: 84907291749     PISSN: 19466234     EISSN: 19466242     Source Type: Journal    
DOI: 10.1126/scitranslmed.3010272     Document Type: Note

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