Genomic sequencing identifies secondary findings in a cohort of parent study participants

PURPOSE: Clinically relevant secondary variants were identified in parents enrolled with a child with developmental delay and intellectual disability. METHODS: Exome/genome sequencing and analysis of 789 ‘unaffected’ parents was performed. RESULTS: Pathogenic/likely pathogenic variants were identifi...

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Detalles Bibliográficos
Autores principales: Thompson, Michelle L., Finnila, Candice R., Bowling, Kevin M., Brothers, Kyle B., Neu, Matthew B., Amaral, Michelle D., Hiatt, Susan M., East, Kelly M., Gray, David E., Lawlor, James M.J., Kelley, Whitley V., Lose, Edward J., Rich, Carla A., Simmons, Shirley, Levy, Shawn E., Myers, Richard M., Barsh, Gregory S., Bebin, E. Martina, Cooper, Gregory M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6185813/
https://www.ncbi.nlm.nih.gov/pubmed/29790872
http://dx.doi.org/10.1038/gim.2018.53

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6185813/
https://www.ncbi.nlm.nih.gov/pubmed/29790872
http://dx.doi.org/10.1038/gim.2018.53

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