AUB ScholarWorks

Browsing by Author "Cabet F."

Browsing by Author "Cabet F."

Sort by: Order: Results:

  • Cystic fibrosis: A new mutation in the Lebanese population 
    Farra C.; Medawar R.; Mroueh S.; Souaid M.; Cabet F.; Awwad J. (AMSTERDAMPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS, 2008)
    Background: Cystic fibrosis is the most common autosomal recessive disorder in Caucasians. Little has been reported on its occurrence in Arab and Lebanese populations where mutation distribution seems to differ from that ...
  • Mutational spectrum of cystic fibrosis in the Lebanese population 
    Farra C.; Menassa R.; Awwad J.; Morel Y.; Salameh P.; Yazbeck N.; Majdalani M.; Wakim R.; Yunis K.; Mroueh S.; Cabet F. (AMSTERDAMPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS, 2010)
    Background: Cystic fibrosis (CF) is the most common autosomal recessive disease in Caucasians; it is however, considered to be rare in the Arab populations. Reports of the cystic fibrosis transmembrane regulator (CFTR) ...
  • Novel human pathological mutations. Gene symbol: CFTR. Disease: cystic fibrosis. 
    Farra C.; Medawar R.; Cabet F.; Mroueh S.; Souaid M.; Hourani H.; Mounsef C.; Ashkar H.; Awwad J. (, 2007)
    [No abstract available]

Search AUB ScholarWorks

Browse

My Account