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Article

15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridization.

American journal of medical genetics. Part A - 1 Aug 2008

Brunetti-Pierri Nicola, Sahoo Trilochan, Frioux Sarah, Chinault Craig, Zascavage Roxanne, Cheung Sau-Wai, Peters Sarika, Shinawi Marwan

Abstract excerpt

We report on a detailed phenotypic characterization of two patients with novel de novo deletions involving 15q13q14, a chromosomal region immediately distal to the Prader-Willi/Angelman syndrome critical interval. Both cases were detected by the clinical array-based comparative genomic hybridization (array-CGH) and were precisely delineated through the high-density Agilent 244 K oligonucleotide array. The...

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Identifiers

PMID: 18561338
DOI: 10.1002/ajmg.a.32324

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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