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Targeted Next-Generation Sequencing in Patients with Suggestive X-Linked Intellectual Disability.
Genes (Basel). 2020 Jan 2;11(1):51. doi: 10.3390/genes11010051.
Genes (Basel). 2020.
PMID: 31906484
Free PMC article.
A novel nonsense homozygous variant in the NLGN1 gene found in a pair of monozygotic twin brothers with intellectual disability and autism.
Tejada MI, Elcoroaristizabal X, Ibarluzea N, Botella MP, de la Hoz AB, Ocio I.
Tejada MI, et al. Among authors: ocio i.
Clin Genet. 2019 Feb;95(2):339-340. doi: 10.1111/cge.13466. Epub 2018 Nov 20.
Clin Genet. 2019.
PMID: 30460678
No abstract available.
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[Paraneoplastic opsoclonus myoclonus ataxia syndrome].
Aguilera Albesa S, Botella MP, Salado C, Bosque A, Ocio I, Montiano JI.
Aguilera Albesa S, et al. Among authors: ocio i.
An Sist Sanit Navar. 2009 Jan-Apr;32(1):91-5.
An Sist Sanit Navar. 2009.
PMID: 19430515
Free article.
Spanish.
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