NICHD Research Initiative in Newborn Screening

Mental Retardation and Developmental Disabilities Research Reviews

Volumn 12, Issue 4, 2006, Pages 301-304

  Alexander, Duane ^a   Hanson, James W ^a  

^a EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

Author keywords

Genetics; Newborn screening; Public health; Technology; Therapeutics

Indexed keywords

COMMUNITY; EDUCATION; FAMILY; HEALTH CARE SYSTEM; HUMAN; NEWBORN; NEWBORN SCREENING; OUTCOME ASSESSMENT; PRIORITY JOURNAL; QUALITY CONTROL; RESEARCH; REVIEW; SCREENING TEST; TECHNOLOGY;

DIFFUSION OF INNOVATION; FORECASTING; HEALTH SERVICES NEEDS AND DEMAND; HUMANS; INFANT, NEWBORN; NATIONAL INSTITUTES OF HEALTH (U.S.); NEONATAL SCREENING; RESEARCH; UNITED STATES;

EID: 33846009121     PISSN: 10804013     EISSN: 10982779     Source Type: Journal    
DOI: 10.1002/mrdd.20131     Document Type: Review

References (5)

1. American College of Medical Genetics Newborn Screening Expert Group. 2006. Newborn screening: toward a uniform screening panel and system: Executive summary. Pediatrics 117:296-307.
2. Collins FS, Green ED, Guttmacher AB, et al. 2003. A blueprint for the genomic era. Nature 422:835-847.
3. Guthrie R. 1962. Screening for "inborn errors of metabolism" in the newborn infant-a multiple test program. Birth Defects Orig Art Ser 4:92-98.
4. National Academy of Sciences. 1975. Generic screening: programs, principles, and research. Washington, DC: National Academy of Sciences.
5. Report of a WHO Scientific Group. 1968. Screening for inborn errors of metabolism. WHO Tech Rep Ser 401:1-57.