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Article

Parental origin of chromosome 5 deletions in the cri‐du‐chat syndrome

1 Sept 1990

Abstract excerpt

The parental origin of de novo deletions leading to the cri-du-chat syndrome has been investigated. Since the cri-du-chat syndrome is correlated with deletions involving the short arm of chromosome 5 (5p), DNA fragments known to detect restriction fragment length polymorphisms (RFLPs) along 5p were used to establish whether the paternal or the maternal chromosome had suffered the deletion. In cases where only one...

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Share to Chromosomal and Genetic Variations
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Identifiers

PMID: 1978567
DOI: 10.1002/ajmg.1320370119

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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.

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