Article
SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Dec 2013
An Yu, Amr Sami S, Torres Alcy, Weissman Laura, Raffalli Peter, Cox Gerald, Sheng Xiaoming, Lip Va, Bi Weimin, Patel Ankita, Stankiewicz Pawel, Wu Bai-Lin, Shen Yiping
Abstract excerpt
20p13 telomeric/subtelomeric deletions are clinically significant but are currently under-investigated. So far only five molecularly delineated cases have been reported in literature and no candidate genes have been sufficiently implicated. Here, we present six new deletion cases identified by chromosomal microarray analysis (CMA). We also review 32 cases combined from literature and databases. We found that most...
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