Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in neonatal hypertrypsinaemia with normal sweat test

Míreanna Comhchosúla

• Protracted neonatal hypertrypsinogenaemia, normal sweat chloride, and cystic fibrosis
  le: Castellani, C, et al.
  Foilsithe: (2000)
• Cystic fibrosis mutations in heterozygous newborns with hypertrypsinemia and low sweat chloride.
  le: Castellani, C, et al.
  Foilsithe: (1999)
• CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test.
  le: Castellani, C, et al.
  Foilsithe: (1997)
• High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia.
  le: Gomez Lira M, et al.
  Foilsithe: (2000)
• Sweat testing in newborns positive to neonatal screening for cystic fibrosis
  le: Taccetti, G, et al.
  Foilsithe: (2004)