Cystic fibrosis mutations in heterozygous newborns with hypertrypsinemia and low sweat chloride.

Liknande verk

• 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)
• Protracted neonatal hypertrypsinogenaemia, normal sweat chloride, and cystic fibrosis
  av: Castellani, C, et al.
  Publicerad: (2000)
• CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test.
  av: Castellani, C, et al.
  Publicerad: (1997)
• Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in neonatal hypertrypsinaemia with normal sweat test
  av: CASTELLANI, C., et al.
  Publicerad: (2001)
• Comparison of Quantitative Sweat Chloride Methods after Positive Newborn Screen for Cystic Fibrosis
  av: Laguna, Theresa A., et al.
  Publicerad: (2012)