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

Characterization of a novel deletion causing (deltabeta)0-thalassemia in a Thai family.

American journal of hematology - 1 Feb 2007

Svasti Saovaros, Paksua Surachate, Nuchprayoon Issarang, Winichagoon Pranee, Fucharoen Suthat

Abstract excerpt

A novel deletion of the human beta-globin gene cluster associated with the increased level of fetal hemoglobin (Hb F) in adult life has been demonstrated in a Thai family. A Thai girl who was mistakenly diagnosed as beta-thalassemia/HbE is found to be the compound heterozygote of this mutation and Hb E. The heterozygous father had mild hypochromic and microcytic red blood cells and a high level of Hb F (23.2%)....

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 Family
Share to Fetal Hemoglobin

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

Share to Globins

Share to Homozygote

Share to Multigene Family

Share to Sequence Deletion

Share to Thailand

Source

Identifiers

PMID: 17034028
DOI: 10.1002/ajh.20781

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

Characterization of a novel deletion causing (deltabeta)0-thalassemia in a Thai family.PMID 17034028Read ↗

Severe beta(0) thalassemia/hemoglobin E disease caused by de novo 22-base pair duplication in the paternal allele of beta globin gene.Semantic proximity Read ↗

Beta zero-thalassemia in a Thai family is caused by a 3.4 kb deletion including the entire beta-globin gene.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 ↗

Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.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 ↗

Identification and molecular characterization of four new large deletions in the beta-globin gene cluster.Semantic proximity Read ↗

α&#8304;-Thalassemia and Related Disorders in Northeast Thailand: A Molecular and Hematological CharacterizationSemantic proximity Read ↗

Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.Semantic proximity Read ↗

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

A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization.Semantic proximity Read ↗

[Prenatal diagnosis of Thailand deletion of alpha-thalassemia 1].Semantic proximity Read ↗

Molecular characterization of deletional forms of beta-thalassemia in Taiwan.Semantic proximity Read ↗

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