A model program to increase translation of rare disease genetic tests: Collaboration, education, and test translation program

Genetics in Medicine

Volumn 10, Issue 5, 2008, Pages 343-348

  Faucett, William Andrew ^a   Hart, Suzanne ^b   Pagon, Roberta A ^c   Neall, Lisa Forman ^d   Spinella, Giovanna ^e  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c UNIVERSITY OF WASHINGTON   (United States)

^d NATIONAL INSTITUTES OF HEALTH   (United States)

^e NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

CETT; CLIA; Model program; Rare diseases; Test translation

Indexed keywords

ARTICLE; CLINICAL LABORATORY; CLINICAL RESEARCH; GENETIC ANALYSIS; GENETIC DATABASE; GENETIC DISORDER; GENOTYPE; HEALTH CARE ORGANIZATION; HEALTH EDUCATION; HEALTH PROGRAM; MEDICAL INFORMATION; MODEL; RARE DISEASE;

GENETIC DISEASES, INBORN; GENETIC TECHNIQUES; HUMANS; LABORATORY PERSONNEL; MODELS, ORGANIZATIONAL; PROGRAM DEVELOPMENT; RARE DISEASES;

EID: 44449135622     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/GIM.0b013e318172837c     Document Type: Article

References (2)

1. World Wide Web page Centers for Disease Control and Prevention. Available at: http://wwwn.cdc.gov/dls/genetics/RareDiseaseConf.aspx.
2. World Wide Web page NIH Office of Rare Diseases CETT Program. Available at: http://www.cettprogram.org/.