F. Ouali

α-Thalassaemia in Tunisia: some epidemiological and molecular data

Hajer Siala, F. Ouali, Taïeb Messaoud et al. · Journal of Genetics · 2008 · 22 citations

Epidemiology, Hematology, Molecular Data +2

Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients

Latifa Jouini, Chaîma Sahli, Naouel Laaouini et al. · Molecular Biology Reports · 2013 · 15 citations

Immunohematology, Laboratory Hematology, Clinical Expression +8

Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association

Naouel Laouini, Afsha Bibi, H. Ben Ammar et al. · Molecular Biology Reports · 2012 · 14 citations

Glucose-6-phosphate Dehydrogenase Deficiency, Metabolic Disorder, Metabolic Disease +6

Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience

F. Ouali, Hajer Siala, Afsha Bibi et al. · International Journal of Laboratory Hematology · 2016 · 13 citations

A Novel α‐Thalassemia Nonsense Mutation in Codon 23 of the α2‐Globin Gene (<i>G</i>AG→<i>T</i>AG) in a Tunisian Family

Hajer Siala, Slaheddine Fattoum, Taïeb Messaoud et al. · Hemoglobin · 2004 · 10 citations

Genetics, Molecular Biology, Molecular Genetics +16