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

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

Blood cells, molecules & diseases - 1 Apr 2014

Chaibunruang Attawut, Karnpean Rossarin, Fucharoen Goonnapa, Fucharoen Supan

Abstract excerpt

AEBart's disease is a thalassemia intermedia usually characterized by the interaction of α(0)-thalassemia with either deletional or non-deletional α(+)-thalassemia in Hb E heterozygote. Genotypic and phenotypic features are heterogeneous. We studied the hematologic and molecular characteristics of this disease in a cohort of 173 Thai patients encountered at our center in northeast Thailand. Hemoglobin and DNA...

Read the complete abstract on PubMed

Topics

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

Share to Epistasis, Genetic
Share to Gene Order

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

Share to Genetic Heterogeneity

Share to Hemoglobin E

Share to Hemoglobin H

Share to Hemoglobins, Abnormal

Share to Thailand

Share to Thalassemia

Source

Identifiers

PMID: 24314747
DOI: 10.1016/j.bcmd.2013.11.006

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

Genetic heterogeneity of hemoglobin AEBart's disease: a large cohort data from a single referral center in northeast Thailand.PMID 24314747Read ↗

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

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

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

A large cohort of hemoglobin variants in Thailand: molecular epidemiological study and diagnostic consideration.Semantic proximity Read ↗

Phenotype and Genotype in a Cohort of 312 Adult Patients with Nontransfusion-Dependent Thalassemia in Northeast 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 and hematological studies in a large cohort of α(0)-thalassemia in northeast Thailand: data from a single referral center.Semantic proximity Read ↗

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

A large cohort of β(+)-thalassemia in Thailand: molecular, hematological and diagnostic considerations.Semantic proximity Read ↗

Clinical phenotypes and molecular diagnosis in a hitherto interaction of Hb E/beta thalassemia syndrome (beta(E)/beta(-31), (A -->G)).Semantic proximity Read ↗

Clinical and hematological characteristics of beta-plus thalassemia and uncommon beta-chain hemoglobin variants in Northern Thailand.Semantic proximity Read ↗

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