Chantal Farra

Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype–phenotype correlations

José A. Caparrós‐Martín, Verónica Pulido, Víctor Martínez‐Glez et al. · American Journal of Medical Genetics Part A · 2013 · 54 citations

Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions

Helene Puehringer, Hossein Najmabadi, Hai‐Yang Law et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 2007 · 47 citations

Mutational spectrum of cystic fibrosis in the Lebanese population

Chantal Farra, Rita Menassa, Johnny Awwad et al. · Journal of Cystic Fibrosis · 2010 · 43 citations · Full text

Fibrosis, Mendelian Disorder, Genetic Disorder +4

Acceptance of preimplantation genetic diagnosis for β‐thalassemia in Lebanese women with previously affected children

Chantal Farra, Anwar H. Nassar, Ihab M. Usta et al. · Prenatal Diagnosis · 2008 · 25 citations

Implementation of an intensive risk‐stratified treatment protocol for children and adolescents with acute lymphoblastic leukemia in Lebanon

Samar Muwakkit, Carol Al‐Aridi, Ahmad El Samra et al. · American Journal of Hematology · 2012 · 24 citations · Full text

Hematological Malignancy, Primary Care, Adolescent Medicine +14