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

[Wiskott-Aldrich syndrome with special phenotypes: report of 3 cases].

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics - 1 Feb 2017

He Jian-Xin, Chen Guan-Rong, Xu Bao-Ping, Liu Xiu-Yun, Gui Jin-Gang, Shen Kun-Ling, Jiang Zai-Fang, Lau Yu-Lung

Abstract excerpt

No abstract is available from the source.

Topics

Join the communities discussing this publication.

Infant
Phenotype
Wiskott-Aldrich Syndrome

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 28202128
PMCID: PMC7389471

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Wiskott-Aldrich syndrome with special phenotypes: report of 3 cases].PMID 28202128Read ↗

[Wiskott-Aldrich syndrome: recent progress in diagnosis and treatment].Semantic proximity Read ↗

[Wiskott-Aldrich syndrome].Semantic proximity Read ↗

Wiskott-Aldrich syndrome: current research concepts.Semantic proximity Read ↗

Gene symbol: WAS. Disease: Wiskott-Aldrich syndrome.Semantic proximity Read ↗

Gene symbol: WAS. Disease: Wiskott-Aldrich syndrome.Semantic proximity Read ↗

Gene symbol: WAS. Disease: Wiskott-Aldrich syndrome.Semantic proximity Read ↗

[Spontaneous reversion mutation of Wiskott-Aldrich syndrome pathogenic gene and its clinical implications].Semantic proximity Read ↗

[Molecular and clinical features of SCA 7].Semantic proximity Read ↗

[Aarskog-Scott syndrome].Semantic proximity Read ↗

[William's syndrome: a phenotypic diagnosis].Semantic proximity Read ↗

[Wiskott-Aldrich Syndrome: An updated review].Semantic proximity Read ↗

[Clinical features and genotype analysis of 132 patients with Wiskott-Aldrich syndrome].Semantic proximity Read ↗

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