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Article

Cri du chat syndrome.

Journal of postgraduate medicine - 1 Jan 2000

Iyer S L, Duraiswamy A, Kher A S, Joshi S, Bharucha B A, Kanade S

Abstract excerpt

Three cases of cri du chat syndrome with varying ages of presentation are compared and contrasted to highlight the clinical features and evolution of the phenotype with time.

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Share to Chromosome Deletion
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9715326

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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[Accidental finding of a cri du chat syndrome in an adult patient by means of array-CGH].Semantic proximity Read ↗

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Deletion of the Telomerase Reverse Transcriptase Gene and Haploinsufficiency of Telomere Maintenance in Cri du Chat SyndromeSemantic proximity Read ↗

Phenotypic and phoniatric findings in mosaic cri du chat syndrome.Semantic proximity Read ↗

Cri du chat mosaicism: an unusual case of partial deletion and partial deletion/ duplication of the short arm of chromosome 5, leading to an unusual cri du chat phenotype.Semantic proximity Read ↗

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