Clinical and molecular aspects of haemoglobinopathies in Tunisia.

doi:10.1016/j.cccn.2003.10.022

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Article

Clinical and molecular aspects of haemoglobinopathies in Tunisia.

Clinica chimica acta; international journal of clinical chemistry - 1 Feb 2004

Haj Khelil Amel, Laradi Sandrine, Miled Abdelhedi, Omar Tadmouri Ghazi, Ben Chibani Jemni, Perrin Pascale

Abstract excerpt

BACKGROUND: For the last two decades, studies on the population genetics of Tunisians have focused on variations of protein and genetic markers. Results confirmed the genetic heterogeneity of Tunisians caused by the admixtures with migratory human groups arriving mainly from Africa, Europe, and Asia. These studies also allowed the screening of rare mutants and many haemoglobin variants. METHODS: The present study...

Topics

Anemia, Sickle Cell
DNA Mutational Analysis
Electrophoresis, Polyacrylamide Gel
Haplotypes
Hemoglobinopathies
Heterozygote
Homozygote
Humans
Mutation
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Prenatal Diagnosis
Tunisia
beta-Thalassemia

Source

Open in PubMed

Identifiers

PMID: 14734204
DOI: 10.1016/j.cccn.2003.10.022

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