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

Eight-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta khon kaen) with an inclusion body beta-thalassemia trait.

Blood - 15 Jul 1991

Fucharoen G, Fuchareon S, Jetsrisuparb A, Fukumaki Y

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Base Sequence
Share to Child, Preschool
Share to Chromosome Deletion

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

Share to Globins

Share to Molecular Sequence Data

Share to Thalassemia

Source

Identifiers

PMID: 2070092

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

Eight-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta khon kaen) with an inclusion body beta-thalassemia trait.PMID 2070092Read ↗

A single nucleotide deletion in codon 123 of the beta-globin gene causes an inclusion body beta-thalassaemia trait: a novel elongated globin chain beta Makabe.Semantic proximity Read ↗

A deletion of 11 bp (CD 131-134) in exon 3 of the beta-globin gene produces the phenotype of inclusion body beta-thalassemia.Semantic proximity Read ↗

A novel 4.9 Kb deletion at beta-globin gene is identified by the third-generation sequencing: Case report from Baoan, ChinaSemantic proximity Read ↗

A spontaneous mutation produced a novel elongated beta-globin chain structural variant (Hb Agnana) with a thalassemia-like phenotype.Semantic proximity Read ↗

A rare complex rearrangement in the β-globin gene cluster causing a novel homozygous G γ(A γδβ)0 -thalassemia.Semantic proximity Read ↗

A novel mutation (nonsense beta 127) in exon 3 of the beta globin gene produces a variable thalassaemic phenotype.Semantic proximity Read ↗

A novel 506 kb deletion causing εγδβ thalassemiaSemantic proximity Read ↗

Characterization of a novel deletion causing beta-thalassemia major in an Afghan family.Semantic proximity Read ↗

Mild Hb S-beta(+)-thalassemia with a deletion of five nucleotides at the polyadenylation site of the beta-globin gene.Semantic proximity Read ↗

A mutation of CDS 82/83 (-G) observed in a Yugoslavian family with a heterozygosity for beta-thalassemia.Semantic proximity Read ↗

Dominantly Inherited beta-Thalassemia.Semantic proximity Read ↗

Dominant thalassemia-like phenotypes associated with mutations in exon 3 of the beta-globin gene.Semantic proximity Read ↗

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