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Article

A rare chromosome 5 heterochromatic variant derived from insertion of 9qh satellite 3 sequences.

Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology - 1 Aug 1998

Doneda L, Gandolfi P, Nocera G, Larizza L

Abstract excerpt

A rare chromosome 5 heterochromatic variant not linked to any clinical sign was identified in a three-generation family. After performing conventional cytogenetics characterization, fluorescence in situ hybridization of D9Z1 indicated that the unusually large qh region of chromosome 5 originated from 9qh, whereas the centromere of the variant chromosome was 5-specific as demonstrated by primed in situ DNA...

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Source

Identifiers

PMID: 9872671
DOI: 10.1023/a:1009237608514

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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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