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

Hematological phenotype of the IVS-I-5 (G > C) beta-thalassemia mutation and assessment of Iran's national screening criteria.

Hemoglobin - 1 Jan 2008

Eshghi Peyman, Rashidi Armin, Zadeh-Vakili Azita, Miri-Moghadam Ebrahim

Abstract excerpt

In a recent study, we demonstrated that, in the Iranian province of Sistan-Baluchestan (S-B), the IVS-I-5 (G > C) beta-thalassemia (beta-thal) mutation is highly prevalent. In the present article we report the hematological phenotype as measured in 289 carriers of this mutation. We evaluate the use of MCV and MCH parameters as proposed in Iran's national screening guidelines for use in this province. The Hb A(2)...

Read the complete abstract on PubMed

Topics

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

Share to beta-Thalassemia
Share to Hemoglobin A2
Share to Iran

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Source

Identifiers

PMID: 18932068
DOI: 10.1080/03630260802341778

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

Hematological phenotype of the IVS-I-5 (G > C) beta-thalassemia mutation and assessment of Iran's national screening criteria.PMID 18932068Read ↗

Identification of alpha-thalassemia mutations in Iranian individuals with abnormal hematological indices and normal Hb A2.Semantic proximity Read ↗

Identification of alpha-thalassemia mutations in subjects from Eastern Sicily (Italy) with abnormal hematological indices and normal Hb A2.Semantic proximity Read ↗

Molecular characterization and hematological phenotype of Sicilian delta beta-thalassemia .Semantic proximity Read ↗

An unusually frequent beta-thalassemia mutation in an Iranian Province.Semantic proximity Read ↗

An Iranian child with HbQ-Iran [alpha75 (EF4) Asp-->His]/-alpha3.7 kb/IVSII.1 G-->A: first report.Semantic proximity Read ↗

Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.Semantic proximity Read ↗

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

Hematologic phenotype of the mutations IVS1-n6 (T-->C), IVS1-n110 (G-->A), and CD39 (C-->T) in carriers of beta-thalassemia in Greece.Semantic proximity Read ↗

Beta-thalassemia intermedia from southern Iran: IVS-II-1 (G-->A) is the prevalent thalassemia intermedia allele.Semantic proximity Read ↗

Utility and importance of accurate Hb A2 measurements for defining a strategy for β-thalassemia screening: experience in the Balearic Islands, Spain.Semantic proximity Read ↗

Molecular spectrum of beta-thalassemia in the Iranian Province of Hormozgan.Semantic proximity Read ↗

The significance of the hemoglobin A(2) value in screening for hemoglobinopathies.Semantic proximity Read ↗

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