Clinical genetics: Exomes in the clinic

Nature Reviews Genetics

Volumn 14, Issue 12, 2013, Pages 824-

  Flintoft, Louisa ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

COPY NUMBER VARIATION; EXOME; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; INCIDENTAL FINDING; NEUROLOGIC DISEASE; NOTE; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; DNA SEQUENCE; GENETIC DISEASES, INBORN; GENETIC SCREENING; PROCEDURES;

EXOME; GENETIC DISEASES, INBORN; GENETIC TESTING; HUMANS; SEQUENCE ANALYSIS, DNA;

EID: 84887988452     PISSN: 14710056     EISSN: 14710064     Source Type: Journal    
DOI: 10.1038/nrg3620     Document Type: Note

References (1)

1. Yang, Y. et al. Clinical whole-exome sequencing for the diagnosis of Mendelian disorders. N. Engl. J. Med. http://dx.doi.org/10.1056/NEJMoa1306555 (2013)