|
Volumn 346, Issue 7909, 2013, Pages
|
Should we sequence everyone's genome? Yes
|
Author keywords
[No Author keywords available]
|
Indexed keywords
NANOWIRE;
VEMURAFENIB;
WARFARIN;
BIOINFORMATICS;
CARDIOMYOPATHY;
DRUG SENSITIVITY;
FAMILIAL CANCER;
GENE SEQUENCE;
GENETIC ANALYSIS;
GENETIC PREDISPOSITION;
GENETIC VARIABILITY;
GENOMICS;
HEALTH CARE DELIVERY;
HEALTH SERVICE;
HUMAN;
MALARIA;
MEDICAL RESEARCH;
MELANOMA;
MONOGENIC DISORDER;
NOTE;
PRIORITY JOURNAL;
RARE DISEASE;
ARTICLE;
DNA SEQUENCE;
ETHICS;
GENETIC DATABASE;
GENETICS;
HUMAN GENOME;
INFORMED CONSENT;
MEDICAL ETHICS;
PERSONALIZED MEDICINE;
DATABASES, GENETIC;
ETHICS, MEDICAL;
GENETIC PREDISPOSITION TO DISEASE;
GENOME, HUMAN;
GENOMICS;
HUMANS;
INDIVIDUALIZED MEDICINE;
INFORMED CONSENT;
SEQUENCE ANALYSIS, DNA;
MLCS;
MLOWN;
|
EID: 84878288344
PISSN: None
EISSN: 17561833
Source Type: Journal
DOI: 10.1136/bmj.f3133 Document Type: Note |
Times cited : (13)
|
References (5)
|