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

Origin and history of the IVS-I-110 and codon 39 beta-thalassemia mutations in the Lebanese population.

Human biology - 1 Dec 2002

Zahed Laïla, Demont Jocelyne, Bouhass Rachid, Trabuchet Guy, Hänni Catherine, Zalloua Pierre, Perrin Pascale

Abstract excerpt

Using restriction fragment length polymorphisms (RFLPs) and sequence haplotype analysis, we studied the chromosomal background of the beta-globin gene in 31 unrelated Lebanese IVS-I-110 or codon 39 (Cd39) subjects, and five normal betaAbeta/A individuals. Our results are compared with those from similar studies in other parts of the Mediterranean in an attempt to provide insights into historical patterns of...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to beta-Thalassemia
Share to Genetics, Population

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lebanon

Share to Mutation

Share to Polymorphism, Restriction Fragment Length

Source

Identifiers

PMID: 12617492
DOI: 10.1353/hub.2003.0013

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Origin and history of the IVS-I-110 and codon 39 beta-thalassemia mutations in the Lebanese population.PMID 12617492Read ↗

Contribution to the description of the beta-thalassemia spectrum in Tunisia and the origin of mutation diversity.Semantic proximity Read ↗

Molecular basis of beta-thalassemia in Morocco: possible origins of the molecular heterogeneity.Semantic proximity Read ↗

The spectrum of beta-thalassemia mutations in the Oran region of Algeria.Semantic proximity Read ↗

History and origin of beta-thalassemia in Turkey: sequence haplotype diversity of beta-globin genes.Semantic proximity Read ↗

Hemoglobinopathies in North Africa: A ReviewSemantic proximity Read ↗

β-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean Area.Semantic proximity Read ↗

Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.Semantic proximity Read ↗

Genetic heterogeneity of Beta thalassemia in Lebanon reflects historic and recent population migration.Semantic proximity Read ↗

Balearic archipelago: three islands, three beta-thalassemia population patterns.Semantic proximity Read ↗

The frequency of 14 beta-thalassemia mutations in the Arab populations.Semantic proximity Read ↗

The beta-thalassemia mutation/haplotype distribution in the moroccan population.Semantic proximity Read ↗

beta-globin gene cluster haplotypes associated with beta-thalassemia on Corsica island.Semantic proximity Read ↗

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