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Article

Molecular pathology of X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1).

Immunological reviews - 1 Apr 1994

Ramesh N, Fuleihan R, Geha R

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Topics

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Share to Antigens, Differentiation, B-Lymphocyte
Share to Antigens, Differentiation, T-Lymphocyte
Share to CD40 Antigens
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Immunologic Deficiency Syndromes

Source

Identifiers

PMID: 7520884
DOI: 10.1111/j.1600-065x.1994.tb00848.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Click a neighbor to travelStep 1 · 12 closest

Molecular pathology of X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1).PMID 7520884Read ↗

Clinical Phenotypes of Hyper-IgM Syndromes.Semantic proximity Read ↗

[Molecular genetics of X-linked primary immunodeficiencies: advances in diagnosis and prevention].Semantic proximity Read ↗

Update on the hyper immunoglobulin M syndromesSemantic proximity Read ↗

Clinical and genetic analysis of patients with X-linked hyper-IgM syndrome.Semantic proximity Read ↗

Identification of genetic sequence variations associated with the pathogenesis of X-linked hyper-IgM syndromeSemantic proximity Read ↗

X-linked hypogammaglobulinemia and isolated growth hormone deficiency: an update.Semantic proximity Read ↗

Molecular basis for X-linked immunodeficiencies.Semantic proximity Read ↗

Brief report: prenatal diagnosis of X-linked hyper-IgM syndrome.Semantic proximity Read ↗

X-linked hyper-immunoglobulin M syndrome harboring a novel CD40-ligand gene mutation: a case report.Semantic proximity Read ↗

Molecular aspects of somatic hypermutation of immunoglobulin genes.Semantic proximity Read ↗

Deletions in the ligand for CD40 in X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1).Semantic proximity Read ↗

X-linked hyper IgM syndrome: a novel sequence variant associated with an atypical mild phenotype.Semantic proximity Read ↗

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