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Scientific Reports|March 7, 2015
NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversityOssama K Abou Hassan, Akl C Fahed, Manal Batrawi, et al.Cholesterol|August 2, 2017
Premature Valvular Heart Disease in Homozygous Familial HypercholesterolemiaAkl C Fahed, Kamel Shibbani, Rabih R Andary, et al.Pediatric Blood & Cancer|October 15, 2009
Pulmonary hypertension in children and young adults with sickle cell disease: evidence for familial clusteringHanane A Dahoui, Munya N Hayek, Paul J Nietert, et al.Circulation. Genomic and Precision Medicine|September 5, 2020
Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic CardiomyopathyAkl C Fahed, Georges Nemer, Fadi F Bitar, et al.Pageof 4