The authors reply

New England Journal of Medicine

Volumn 371, Issue 12, 2014, Pages 1170-

  Biesecker, Leslie G ^a   Green, Robert C ^b  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EXOME; GENE; GENE FUNCTION; GENE IDENTIFICATION; GENETIC VARIABILITY; GENOME ANALYSIS; HNF1A GENE; HUMAN; LETTER; MEDICAL LITERATURE; MEDICAL RESEARCH; MOLECULAR DYNAMICS; OUTCOME ASSESSMENT; PATIENT ASSESSMENT; PHYSICIAN ATTITUDE; PROFESSIONAL COMPETENCE; PROFESSIONAL KNOWLEDGE; SEQUENCE ANALYSIS; DNA SEQUENCE; GENETIC DISORDER; GENETICS; HUMAN GENOME; NOTE;

EXOME; GENETIC DISEASES, INBORN; GENOME, HUMAN; HUMANS; SEQUENCE ANALYSIS, DNA;

EID: 84907395628     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMc1408914     Document Type: Letter

References (1)

1. Green RC, Berg JS, Grody WW, et al. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med 2013;15:565-74.