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

Male X-chromosome mosaicism leading to carrier phenotype and inheritance of chronic granulomatous disease.

The journal of allergy and clinical immunology. In practice - 1 Jan 2000

Harris Stephanie, Braggins Helen, van Leeuwen Karin, Gilmour Kimberly, Buckland Matthew S, Roos Dirk, Lowe David M

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 Genes, X-Linked
Share to Genetic Testing
Share to Granulomatous Disease, Chronic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hematopoiesis

Share to High-Throughput Nucleotide Sequencing

Share to Mosaicism

Share to NADPH Oxidase 2

Share to Neutrophil Activation

Source

Identifiers

PMID: 29410207
DOI: 10.1016/j.jaip.2018.01.017

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Male X-chromosome mosaicism leading to carrier phenotype and inheritance of chronic granulomatous disease.PMID 29410207Read ↗

Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease.Semantic proximity Read ↗

Gene symbol: CYBB. Disease: X-linked chronic granulomatous disease.Semantic proximity Read ↗

Hematologically important mutations: X-linked chronic granulomatous disease--an update.Semantic proximity Read ↗

Hematologically important mutations: X-linked chronic granulomatous disease (second update).Semantic proximity Read ↗

Severe phenotype of chronic granulomatous disease presenting in a female with a de novo mutation in gp91-phox and a non familial, extremely skewed X chromosome inactivationSemantic proximity Read ↗

Expanding the Clinical Phenotype of Autosomal Recessive Chronic Granulomatous Disease.Semantic proximity Read ↗

Rapid Genetic Analysis of X-Linked Chronic Granulomatous Disease by High-Resolution MeltingSemantic proximity Read ↗

Expanding the Clinical Phenotype of Chronic Granulomatous Disease: a Female Patient with a De Novo Mutation in CYBB.Semantic proximity Read ↗

Rare XXY/XX mosaicism in a phenotypic male presenting as cystic hygroma in the first trimester.Semantic proximity Read ↗

Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (first update).Semantic proximity Read ↗

Mouse model for men with klinefelter syndrome: a multifaceted fit for a complex disorder.Semantic proximity Read ↗

Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease.Semantic proximity Read ↗

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