Newborn screening for cystic fibrosis: ensuring more good than harm

This publication has 58 references indexed in Scilit:

• The diagnosis of cystic fibrosis: A consensus statement
  The Journal of Pediatrics, 1998
• Psychological risks of genetically testing children for a hereditary cancer syndrome
  Patient Education and Counseling, 1997
• Neonatal screening for cystic fibrosis: A comparison of two strategies for case detection in 1.2 million babies
  The Journal of Pediatrics, 1995
• Severe Hemolytic Anemia Associated With Vitamin E Deficiency in Infants With Cystic Fibrosis
  Clinical Pediatrics, 1994
• Physiciansʼ knowledge of genetics and genetic tests
  Academic Medicine, 1993
• Progressive malnutrition, severe anemia, hepatic dysfunction, and respiratory failure in a three‐month‐old white girl
  American Journal of Medical Genetics, 1993
• Reproductive decision making of aunts and uncles of a child with cystic fibrosis: Genetic risk perception and attitudes toward carrier identification and prenatal diagnosis
  American Journal of Medical Genetics, 1992
• Pancreatic Function in Infants Identified as Having Cystic Fibrosis in a Neonatal Screening Program
  New England Journal of Medicine, 1990
• Immunoreactive trypsinogen screening for cystic fibrosis: Characterization of infants with a false‐positive screening test
  Pediatric Pulmonology, 1989
• Undiagnosed patients with cystic fibrosis
  Journal of Chronic Diseases, 1980