Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders

Identification of genetic biomarkers associated with autism spectrum disorders (ASDs) could improve recurrence prediction for families with a child with ASD. Here, we describe clinical microarray findings for 253 longitudinally phenotyped ASD families from the Baby Siblings Research Consortium (BSRC...

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Detalles Bibliográficos
Autores principales: D’Abate, L., Walker, S., Yuen, R. K. C., Tammimies, K., Buchanan, J. A., Davies, R. W., Thiruvahindrapuram, B., Wei, J., Brian, J., Bryson, S. E., Dobkins, K., Howe, J., Landa, R., Leef, J., Messinger, D., Ozonoff, S., Smith, I. M., Stone, W. L., Warren, Z. E., Young, G., Zwaigenbaum, L., Scherer, S. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892938/
https://www.ncbi.nlm.nih.gov/pubmed/31801954
http://dx.doi.org/10.1038/s41467-019-13380-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892938/
https://www.ncbi.nlm.nih.gov/pubmed/31801954
http://dx.doi.org/10.1038/s41467-019-13380-2

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