Newborn Screening for Genetic Disorders

Pediatric Clinics of North America

Volumn 56, Issue 3, 2009, Pages 505-513

  Fernhoff, Paul M ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Newborn filter paper card screening; Newborn genetic screening; Newborn metabolic screening

Indexed keywords

BLOOD SAMPLING; CHROMOSOME ABERRATION; CONGENITAL INFECTION; CYSTIC FIBROSIS; DEVELOPMENTAL DISORDER; EARLY DIAGNOSIS; GENETIC DISORDER; GENETIC SCREENING; HEALTH PROGRAM; HIGH RISK POPULATION; HUMAN; INTELLECTUAL IMPAIRMENT; LOW BIRTH WEIGHT; NEWBORN SCREENING; PHENYLKETONURIA; PREMATURITY; PUBLIC HEALTH SERVICE; REVIEW; UNITED STATES; COST BENEFIT ANALYSIS; ECONOMICS; ETHICS; HISTORY; LEGAL ASPECT; NEWBORN;

COST-BENEFIT ANALYSIS; GENETIC DISEASES, INBORN; GENETIC SCREENING; HISTORY, 20TH CENTURY; HUMANS; INFANT, LOW BIRTH WEIGHT; INFANT, NEWBORN; INFANT, PREMATURE; NEONATAL SCREENING; PHENYLKETONURIAS;

EID: 67649124152     PISSN: 00313955     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pcl.2009.03.002     Document Type: Review

References (10)

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