AUB ScholarWorks

Browsing by Author "Cabet, F., Hôpital Debrousse, Laboratoire de Biochimie Pédiatrique, and Department of Endocrinology, Hôpital Mère-Enfant Lyon, France"

Browsing by Author "Cabet, F., Hôpital Debrousse, Laboratoire de Biochimie Pédiatrique, and Department of Endocrinology, Hôpital Mère-Enfant Lyon, France"

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  • 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) ...

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