Prenatal diagnosis of cystic fibrosis

This publication has 23 references indexed in Scilit:

• Three additional DNA polymorphisms in the met gene and D7S8 locus: Use in prenatal diagnosis of cystic fibrosis
  The Journal of Pediatrics, 1987
• A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands
  Nature, 1987
• Prenatal detection of intestinal obstructions, aneuploidy syndromes, and cystic fibrosis by microvillar enzyme assays (disaccharidases, alkaline phosphatase, and glutamyltransferase) in amniotic fluid
  American Journal of Medical Genetics, 1987
• Cystic fibrosis carrier detection using a linked gene probe.
  Journal of Medical Genetics, 1986
• DISACCHARIDASES IN AMNIOTIC FLUID AS POSSIBLE PRENATAL MARKER FOR CYSTIC FIBROSIS
  The Lancet, 1983
• MICROVILLAR PEPTIDASE ACTIVITY IN AMNIOTIC FLUID: POSSIBLE USE IN THE PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS
  The Lancet, 1983
• A Sensitive New Prenatal Test for Sickle-Cell Anemia
  New England Journal of Medicine, 1982
• Genetic diseases: Diagnosis by restriction endonuclease analysis
  The Journal of Pediatrics, 1982
• Enhanced Dexamethasone Resistance in Cystic Fibrosis Cells: Potential Use for Heterozygote Detection and Prenatal Diagnosis
  Science, 1978
• Prospects for prenatal diagnosis of cystic fibrosis: Induction of biochemical abnormalities in fibroblasts from patients with cystic fibrosis by a urinary glycoprotein
  Biochemical and Biophysical Research Communications, 1976