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Article

Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.

European journal of human genetics : EJHG - 1 Apr 2010

Willemsen Marjolein H, Fernandez Bridget A, Bacino Carlos A, Gerkes Erica, de Brouwer Arjan P M, Pfundt Rolph, Sikkema-Raddatz Birgit, Scherer Stephen W, Marshall Christian R, Potocki Lorraine, van Bokhoven Hans, Kleefstra Tjitske

Abstract excerpt

The clinical use of array comparative genomic hybridization in the evaluation of patients with multiple congenital anomalies and/or mental retardation has recently led to the discovery of a number of novel microdeletion and microduplication syndromes. We present four male patients with overlappin...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 19920853
DOI: 10.1038/ejhg.2009.192
PMCID: PMC2987261

Genes

CDH15

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19920853-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.PMID 19920853Read ↗

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