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

A novel telomeric (approximately 285 kb) α-thalassemia deletion leading to a phenotypically unusual HbH disease.

Haematologica - 1 May 2010

Joly Philippe, Lacan Philippe, Labalme Audrey, Bonhomme Elodie, Sanlaville Damien, Francina Alain

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 Adolescent
Share to alpha-Thalassemia
Share to Gene Deletion
Share to Hemoglobin H

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Share to Scoliosis

Share to Telomere

Source

Open in PubMed Open full text

Identifiers

PMID: 19951973
DOI: 10.3324/haematol.2009.018663
PMCID: PMC2864397

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel telomeric (approximately 285 kb) α-thalassemia deletion leading to a phenotypically unusual HbH disease.PMID 19951973Read ↗

The molecular basis of α-thalassemia.Semantic proximity Read ↗

A novel 506 kb deletion causing εγδβ thalassemiaSemantic proximity Read ↗

Novel and unusual deletion-insertion thalassemic mutation in exon 1 of the beta-globin gene.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 ↗

Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.Semantic proximity Read ↗

The Clinical Phenotypes of Alpha Thalassemia.Semantic proximity Read ↗

Molecular basis of α-thalassemia.Semantic proximity Read ↗

The diagnosis and molecular analysis of a novel 27.2 kb deletion causing α0-thalassemia.Semantic proximity Read ↗

A novel α(0) -thalassemia deletion in a Greek patient with HbH disease and β-thalassemia trait.Semantic proximity Read ↗

A Novel εγδβ-Thalassemia Deletion Associated with Severe Anemia at Birth and a β-Thalassemia Intermedia Phenotype Later in Life in Three Generations of a Greek Family.Semantic proximity Read ↗

HBB loss of heterozygosity in the hemopoietic lineage gives rise to an unusual sickle-cell trait phenotype.Semantic proximity Read ↗

Novel α0-Thalassemia Deletion Identified in an Indian Infant with Hb H Disease.Semantic proximity Read ↗

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