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

Liknande verk

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