|
Volumn 501, Issue 7466, 2013, Pages 135-
|
Sequenced from the start
[No Author Info available]
|
Author keywords
[No Author keywords available]
|
Indexed keywords
EDITORIAL;
EXOME;
GENE SEQUENCE;
GENETIC DISORDER;
GENETIC TRAIT;
GENETIC VARIABILITY;
HEALTH CARE SYSTEM;
HUMAN;
HUMAN GENOME;
NEWBORN SCREENING;
PRIORITY JOURNAL;
RESEARCH ETHICS;
SEQUENCE ANALYSIS;
EVALUATION STUDIES AS TOPIC;
FALSE POSITIVE REACTIONS;
GENETIC COUNSELING;
GENETIC PREDISPOSITION TO DISEASE;
GENETIC PRIVACY;
GENETIC TESTING;
GENOME, HUMAN;
GENOMICS;
HEALTH;
HUMANS;
INFANT, NEWBORN;
NEONATAL SCREENING;
PREVENTIVE MEDICINE;
UNITED STATES;
|
EID: 84884165423
PISSN: 00280836
EISSN: 14764687
Source Type: Journal
DOI: 10.1038/501135a Document Type: Editorial |
Times cited : (3)
|
References (0)
|