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

Podobné jednotky

• High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia.
  Autor: Gomez Lira M, a další
  Vydáno: (2000)
• Protracted neonatal hypertrypsinogenaemia, normal sweat chloride, and cystic fibrosis
  Autor: Castellani, C, a další
  Vydáno: (2000)
• CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test.
  Autor: Castellani, C, a další
  Vydáno: (1997)
• Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in neonatal hypertrypsinaemia with normal sweat test
  Autor: CASTELLANI, C., a další
  Vydáno: (2001)
• Comparison of Quantitative Sweat Chloride Methods after Positive Newborn Screen for Cystic Fibrosis
  Autor: Laguna, Theresa A., a další
  Vydáno: (2012)