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

Deletion of chromosome 20 in bone marrow of patients with S hwachman‐ D iamond syndrome, loss of the EIF6 gene and benign prognosis

1 Feb 2012

Abstract excerpt

The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.

Read the complete abstract on PubMed

Topics

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

Share to Blood disorders and treatments
Share to Immunodeficiency and Autoimmune Disorders
Share to Pneumocystis jirovecii pneumonia detection and treatment

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 22295858
DOI: 10.1111/j.1365-2141.2012.09033.x

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

Deletion of chromosome 20 in bone marrow of patients with S hwachman‐ D iamond syndrome, loss of the EIF6 gene and benign prognosisPMID 22295858Read ↗

Shwachman‐Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instabilitySemantic proximity Read ↗

RECQL4-deficient cells are hypersensitive to oxidative stress/damage: Insights for osteosarcoma prevalence and heterogeneity in Rothmund-Thomson syndromeSemantic proximity Read ↗

Gene symbol: RPS19. Disease: Diamond-Blackfan anaemia.Semantic proximity Read ↗

Refining the phenotype associated with biallelic DNAJC21 mutations.Semantic proximity Read ↗

Compendium of FAM 46C gene mutations in plasma cell dyscrasiasSemantic proximity Read ↗

Stüve-Wiedemann syndrome: LIFR and associated cytokines in clinical course and etiology.Semantic proximity Read ↗

RPS19 mutations in patients with Diamond-Blackfan anemia.Semantic proximity Read ↗

Tumor suppressor TNFAIP3 (A20) is frequently deleted in Sézary syndromeSemantic proximity Read ↗

The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocation.Semantic proximity Read ↗

Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature.Semantic proximity Read ↗

Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions.Semantic proximity Read ↗

6q27 subtelomeric deletions: Is there a specific phenotype?Semantic proximity Read ↗

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