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

β-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean Area.

Hemoglobin - 1 Jan 2016

Cherry Laudy, Calo Carla, Talmaci Rodica, Perrin Pascale, Gavrila Lucian

Abstract excerpt

The purpose of this meta-study was to investigate β-thalassemia (β-thal) mutations and their chromosomal background in order to highlight the origin and spread of thalassemia alleles in the European and Mediterranean areas. Screening of more than 100 new Romanian β-thal alleles was also conducted. The results suggest an ancient introduction of mutations at codon 39 (C > T) (HBB: c.118C > T) and IVS-I-6 (T > C)...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Amino Acid Substitution
Share to Codon

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

Share to Gene Frequency

Share to Haplotypes

Share to Linkage Disequilibrium

Share to Mutation

Share to Polymorphism, Restriction Fragment Length

Source

Identifiers

PMID: 26711012
DOI: 10.3109/03630269.2015.1124113

Genes

HBB

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

β-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean Area.PMID 26711012Read ↗

Molecular profiling of thalassemia in Southeastern Romania.Semantic proximity Read ↗

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

The Spectrum of β-Thalassemia Mutations in the Population Migration in Lebanon: A 6-Year Retrospective Study.Semantic proximity Read ↗

Molecular heterogeneity of beta-thalassemia in Algeria: how to face up to a major health problem.Semantic proximity Read ↗

Two new β+ -thalassemia mutation [β -56 (G → C); HBBc. -106 G → C] and [β -83 (G → A); HBBc. -133 G → A] described among the Tunisian population.Semantic proximity Read ↗

Spectrum of β-thalassemia mutations in the eastern province of Saudi Arabia.Semantic proximity Read ↗

Molecular Characterization of β-Thalassemia in the Czech and Slovak Populations: Mediterranean, Asian and Unique Mutations.Semantic proximity Read ↗

Scanning of beta-globin gene for identification of beta-thalassemia mutation in Romanian population.Semantic proximity Read ↗

Beta Globin Gene Cluster Haplotypes in Beta Thalassemia in the Kurdistan Region of Iraq.Semantic proximity Read ↗

Thalassemias and other hemoglobinopathies in the Republic of Macedonia.Semantic proximity Read ↗

β-thalassemia distribution in the old world: a historical standpoint of an ancient diseaseSemantic proximity Read ↗

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

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