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Article

An additional case of the recurrent 15q24.1 microdeletion syndrome and review of the literature.

Twin research and human genetics : the official journal of the International Society for Twin Studies - 1 Aug 2011

L Ng Ivy S, Chin Wai-Hoe, P Lim Eileen C, Tan Ene-Choo

Abstract excerpt

We report a 9-year-old girl with 3 Mb interstitial deletion of chromosome 15q24 identified by oligonucleotide array comparative hybridization. She is of Chinese ancestry and shared some typical features of previously reported 15q24 deletion cases such as mild dysmorphism with developmental and sp...

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Share to Abnormalities, Multiple
Share to Chromosome Deletion
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 21787116
DOI: 10.1375/twin.14.4.333

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21787116-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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