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

The diverse molecular basis and hematological features of Hb H and AEBart's diseases in Northeast Thailand.

Acta haematologica - 1 Jan 2004

Boonsa Supap, Sanchaisuriya Kanokwan, Fucharoen Goonnapa, Wiangnon Surapon, Jetsrisuparb Arunee, Fucharoen Supan

Abstract excerpt

We defined the molecular basis and correlated the hematological phenotypes with the globin genotypes in 52 patients with Hb H disease and 29 patients with AEBart's disease of northeast Thailand. Among the former group, the most prevalent molecular defect was found to be the interaction of alpha-thalassemia 1 (SEA type) with the Hb Constant Spring (Hb CS; 35 of 52 patients), followed by the deletion of three...

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 Child, Preschool

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

Share to DNA Mutational Analysis

Share to Hematologic Tests

Share to Molecular Epidemiology

Share to Sequence Deletion

Share to Thailand

Share to Thalassemia

Source

Identifiers

PMID: 15034236
DOI: 10.1159/000076523

Genes

SEA

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

The diverse molecular basis and hematological features of Hb H and AEBart's diseases in Northeast Thailand.PMID 15034236Read ↗

Genetic heterogeneity of hemoglobin AEBart's disease: a large cohort data from a single referral center in northeast Thailand.Semantic proximity Read ↗

Molecular and clinical features of Hb H disease in northern Thailand.Semantic proximity Read ↗

Molecular Characterization of Hb H and AEBart’s Diseases in Thai Children: Phramongkutklao Hospital Experiences.Semantic proximity Read ↗

Molecular and hematological profiles of hemoglobin EE disease with different forms of alpha-thalassemia.Semantic proximity Read ↗

Molecular and hematologic features of hemoglobin E heterozygotes with different forms of alpha-thalassemia in Thailand.Semantic proximity Read ↗

A large cohort of Hb H disease in northeast Thailand: A molecular revisited, diverse genetic interactions and identification of a novel mutation.Semantic proximity Read ↗

Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in ThailandSemantic proximity Read ↗

Hemoglobin Q-Thailand related disorders: origin, molecular, hematological and diagnostic aspects.Semantic proximity Read ↗

Clinical phenotypes and genotypes diagnosis of thalassemia in children.Semantic proximity Read ↗

Clinical features and molecular analysis in Thai patients with HbH disease.Semantic proximity Read ↗

Phenotype and Genotype in a Cohort of 312 Adult Patients with Nontransfusion-Dependent Thalassemia in Northeast Thailand.Semantic proximity Read ↗

Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand.Semantic proximity Read ↗

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