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Article

A CGH array study in nonsyndromic (primary) autism patients: deletions on 16p13.11, 16p11.2, 1q21.1, 2q21.1q21.2, and 8p23.1.

Turkish journal of medical sciences - 1 Jan 2015

Gümüşlü Kudret Esen, Savli Hakan, Sünnetçi Deniz, Çine Naci, Kara Bülent, Eren Keskin Seda, Akkoyunlu Ramis Ufuk

Abstract excerpt

BACKGROUND/AIM: To detect specific molecular changes of DNA level in primary autism patients by using whole genome CGH array technology. MATERIALS AND METHODS: A cohort of 35 primary autism patients received clinical genetic testing by using an oligonucleotide-based CGH array platform to test for submicroscopic genomic deletions and duplications. Fluorescent in situ hybridization was performed in seven patients...

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PMID: 26084120

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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