Pages that link to "Q58020445"

The following pages link to Cystic fibrosis mutation analysis: Report from 22 U.K. regional genetics laboratories (Q58020445):

Displaying 10 items.

• Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening (Q28217255) (← links)
• Prenatal screening for cystic fibrosis (Q35171713) (← links)
• Cystic fibrosis newborn screening and detection of carriers (Q35571740) (← links)
• DNA-based carrier screening in the Ashkenazi Jewish population (Q35770579) (← links)
• Correction of mutations within the cystic fibrosis transmembrane conductance regulator by site-directed RNA editing (Q37318051) (← links)
• Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis (Q39585577) (← links)
• Demographics of the UK cystic fibrosis population: implications for neonatal screening (Q44603512) (← links)
• Cationic lipid-mediated CFTR gene transfer to the lungs and nose of patients with cystic fibrosis: a double-blind placebo-controlled trial. (Q45861736) (← links)
• Fecal elastase-1 cut-off levels in the assessment of exocrine pancreatic function in cystic fibrosis (Q80819612) (← links)
• The first case report of double homozygous of 2 different mutations in the CFTR gene in Saudi Arabia (Q91915478) (← links)