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

'Novel' immunodeficiency syndrome may be a previously described entity.

Clinical genetics - 1 Jan 2000

Carpenter N J, Berkel I, Say B

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 Abnormalities, Multiple
Share to Craniosynostoses
Share to Developmental Disabilities
Share to Immunoglobulin G

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Immunologic Deficiency Syndromes

Share to Infections

Share to Microcephaly

Share to X Chromosome

Source

Identifiers

PMID: 10733244
DOI: 10.1034/j.1399-0004.2000.570116.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

'Novel' immunodeficiency syndrome may be a previously described entity.PMID 10733244Read ↗

[Immunodeficiencies: an overview and various diagnostic difficulties].Semantic proximity Read ↗

Common variable immunodeficiency (CVID): new genetic insight and unanswered questions.Semantic proximity Read ↗

Immunodeficiency diagnosis: a Mondrian or Pollock scenario?Semantic proximity Read ↗

A rare primary immunodeficiency.Semantic proximity Read ↗

Unusual presentation of combined immunodeficiency in a child with homozygous DOCK8 mutation.Semantic proximity Read ↗

Intrinsic and extrinsic causes of malignancies in patients with primary immunodeficiency disordersSemantic proximity Read ↗

[Primary immunodeficiency disease based on ITK mutation: report of a case].Semantic proximity Read ↗

Severe combined immunodeficiency syndrome with RAG1 mutation gene - case reportSemantic proximity Read ↗

Immunodeficiency: nobody is immune.Semantic proximity Read ↗

Immunodeficiency-associated viral oncogenesisSemantic proximity Read ↗

Common Variable Immunodeficiency or Late-Onset Combined Immunodeficiency: A New Hypomorphic JAK3 Patient and Review of the Literature.Semantic proximity Read ↗

[Common variable immunodeficiency: one or multiple illnesses? 3 clinical cases].Semantic proximity Read ↗

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