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Article

Inherited 15q24 microdeletion syndrome in twins and their father with phenotypic variability.

European journal of medical genetics - 1 Feb 2015

Samuelsson Lena, Zagoras Theofanis, Hafström Maria

Abstract excerpt

BACKGROUND: Deletions including chromosome 15q24 have been delineated in recent years as a separate syndrome with phenotypic variability. Here we report a familial 15q24 deletion and further contribute to the phenotypic description of this syndrome. METHODS: Molecular karyotyping and description...

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Share to Chromosome Deletion
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Source

Identifiers

PMID: 25527279
DOI: 10.1016/j.ejmg.2014.12.006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25527279-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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