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Article

Inv(10)(p11.2q21.2), a variant chromosome.

Human genetics - 1 Dec 1997

Collinson M N, Fisher A M, Walker J, Currie J, Williams L, Roberts P

Abstract excerpt

We present 33 families in which a pericentric inversion of chromosome 10 is segregating. In addition, we summarise the data on 32 families in which an apparently identical inv(10) has been reported in the literature. Ascertainment was through prenatal diagnosis or with a normal phenotype in 21/33...

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Identifiers

PMID: 9402964
DOI: 10.1007/s004390050609

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Prepared record publication-9402964-2026-09-05.1. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 5 Sept 2026.

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Inv(10)(p11.2q21.2), a variant chromosome.PMID 9402964Read ↗

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