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Article

Transient congenital hypoparathyroidism: Resolution and recurrence in chromosome 22q11 deletion

1 Apr 1996

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8618195
DOI: 10.1016/s0022-3476(96)70372-4

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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

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Transient congenital hypoparathyroidism: Resolution and recurrence in chromosome 22q11 deletionPMID 8618195Read ↗

A novel presentation of a rare chromosome 21q22.2 deletion.Semantic proximity Read ↗

Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements.Semantic proximity Read ↗

Deletion 22q11: Spectrum of Associated DisordersSemantic proximity Read ↗

Review of the Pathophysiology and Clinical Manifestations of 22q11.2 Deletion and Duplication SyndromesSemantic proximity Read ↗

Defining the clinical spectrum of deletion 22q11.2.Semantic proximity Read ↗

Gene Symbol: CASR. Disease: Hyperparathyroidism.Semantic proximity Read ↗

Recurrence of an early postzygotic rescue of an inherited unbalanced translocation resulting in mosaic segmental uniparental isodisomy of chromosome 11q in siblings.Semantic proximity Read ↗

Our evolving understanding of 22q.11 deletion syndrome.Semantic proximity Read ↗

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