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

Bronchiectasis and immune deficiency in an adult patient with deletion 2q37 due to an unbalanced translocation t(2;10)

15 Jan 2009

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 Genomic variations and chromosomal abnormalities
Share to Immunodeficiency and Autoimmune Disorders
Share to Pediatric Hepatobiliary Diseases and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 19272308
DOI: 10.1016/j.ejmg.2009.01.001

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 · 8 closest

Bronchiectasis and immune deficiency in an adult patient with deletion 2q37 due to an unbalanced translocation t(2;10)PMID 19272308Read ↗

Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndromeSemantic proximity Read ↗

Immunological aspects of 22q11.2 deletion syndromeSemantic proximity Read ↗

Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)Semantic proximity Read ↗

A patient with apparently reciprocal translocation and cryptic 10p deletion.Semantic proximity Read ↗

4q35 deletion and 10p15 duplication associated with immunodeficiency.Semantic proximity Read ↗

Trisomy 10p and translocation of 10q to 4p associated with selective dysgenesis of IgA-producing cells in lymphoid tissue.Semantic proximity Read ↗

A Complex Infectious, Inflammatory, and Autoimmune Phenotype Reveals 22q11.2 Deletion Syndrome in an Adult.Semantic proximity Read ↗

Chromosome 22q11.2 deletion syndrome and DiGeorge syndromeSemantic proximity Read ↗

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