Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

alpha-Thalassaemia in Tunisia: some epidemiological and molecular data.

Journal of genetics - 1 Dec 2008

Siala H, Ouali F, Messaoud T, Bibi A, Fattoum S

Abstract excerpt

Unlike the other haemoglobinopathies, few researches have been published concerning alpha-thalassaemia in Tunisia. The aim of the present work is to acquire further data concerning alpha-thalassaemia prevalence and molecular defects spectrum in Tunisia, by collecting and studying several kinds of samples carrying alpha-thalassaemia. The first survey conducted on 529 cord blood samples using cellulose acetate...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to alpha-Thalassemia
Share to Child

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Genotype

Share to Hemoglobin H

Share to Tunisia

Source

Identifiers

PMID: 19147907
DOI: 10.1007/s12041-008-0036-0

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

alpha-Thalassaemia in Tunisia: some epidemiological and molecular data.PMID 19147907Read ↗

Molecular spectrum of alpha-thalassemia in Tunisia: epidemiology and detection at birth.Semantic proximity Read ↗

[Hemoglobinopathies in Tunisia. An updated review of the epidemiologic and molecular data].Semantic proximity Read ↗

Hb H disease among Tunisians: molecular characterization of alpha-thalassemia determinants and hematological findings.Semantic proximity Read ↗

Clinical and molecular aspects of haemoglobinopathies in Tunisia.Semantic proximity Read ↗

Rare hemoglobin variants in Tunisian population.Semantic proximity Read ↗

Molecular basis of alpha-thalassemia in Algeria.Semantic proximity Read ↗

Identification of three different alpha-thalassemic haplotypes: -alpha 3.7, (--)MED and alpha Hph alpha in the same Algerian family.Semantic proximity Read ↗

Mutation Spectrum of Hemoglobinopathies in Tunisia.Semantic proximity Read ↗

Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.Semantic proximity Read ↗

Extended molecular spectrum of beta- and alpha-thalassemia in Oman.Semantic proximity Read ↗

The spectrum of beta-thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy.Semantic proximity Read ↗

Hemoglobinopathies in North Africa: A ReviewSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.