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

Thalassemias and other hemoglobinopathies in the Republic of Macedonia.

Hemoglobin - 1 Jan 2007

Efremov Georgi D

Abstract excerpt

This paper summarizes the results on the epidemiology and molecular basis of thalassemias and other hemoglobinopathies in the Republic of Macedonia. Over the past 40 years, population surveys of more than 22,000 participants (school children and workers) from all over the country, have shown that the average incidence of beta-thalassemia (thal) trait is 2.6%, ranging from less than 1% in the northeast to 10% in...

Read the complete abstract on PubMed

Topics

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

Share to alpha-Thalassemia
Share to beta-Thalassemia
Share to Child, Preschool

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

Share to DNA Mutational Analysis

Share to Hemoglobins, Abnormal

Share to Incidence

Share to Infant, Newborn

Share to Neonatal Screening

Source

Identifiers

PMID: 17365000
DOI: 10.1080/03630260601056726

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

Thalassemias and other hemoglobinopathies in the Republic of Macedonia.PMID 17365000Read ↗

Genotypic Characterization of Hemoglobinopathies in Azerbaijan: A Review of 10 Years at a Referral Center.Semantic proximity Read ↗

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

Sickle cell anemia, sickle cell beta-thalassemia, and thalassemia major in Albania: characterization of mutations.Semantic proximity Read ↗

Molecular and Hematological Analysis of Alpha- and Beta-Thalassemia in a Cohort of Mexican Patients.Semantic proximity Read ↗

A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population.Semantic proximity Read ↗

Molecular characterization of beta-thalassemia in Syria.Semantic proximity Read ↗

Genetic epidemiology of beta-thalassemia in the Maldives: 23 years of a beta-thalassemia screening program.Semantic proximity Read ↗

Hemoglobinopathies.Semantic proximity Read ↗

Genetic Epidemiology, Hematological and Clinical Features of Hemoglobinopathies in IranSemantic proximity Read ↗

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

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

Mutation Spectrum of Hemoglobinopathies in Tunisia.Semantic proximity Read ↗

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