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Whole-exome sequencing for finding de novo mutations in sporadic mental retardation

Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation.

Detalles Bibliográficos
Autor principal: Robinson, Peter N
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046476/
https://www.ncbi.nlm.nih.gov/pubmed/21172032
http://dx.doi.org/10.1186/gb-2010-11-12-144
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author Robinson, Peter N
author_facet Robinson, Peter N
author_sort Robinson, Peter N
collection PubMed
description Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation.
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spelling pubmed-30464762011-12-21 Whole-exome sequencing for finding de novo mutations in sporadic mental retardation Robinson, Peter N Genome Biol Research Highlight Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation. BioMed Central 2010 2010-12-21 /pmc/articles/PMC3046476/ /pubmed/21172032 http://dx.doi.org/10.1186/gb-2010-11-12-144 Text en Copyright ©2010 BioMed Central Ltd
spellingShingle Research Highlight
Robinson, Peter N
Whole-exome sequencing for finding de novo mutations in sporadic mental retardation
title Whole-exome sequencing for finding de novo mutations in sporadic mental retardation
title_full Whole-exome sequencing for finding de novo mutations in sporadic mental retardation
title_fullStr Whole-exome sequencing for finding de novo mutations in sporadic mental retardation
title_full_unstemmed Whole-exome sequencing for finding de novo mutations in sporadic mental retardation
title_short Whole-exome sequencing for finding de novo mutations in sporadic mental retardation
title_sort whole-exome sequencing for finding de novo mutations in sporadic mental retardation
topic Research Highlight
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046476/
https://www.ncbi.nlm.nih.gov/pubmed/21172032
http://dx.doi.org/10.1186/gb-2010-11-12-144
work_keys_str_mv AT robinsonpetern wholeexomesequencingforfindingdenovomutationsinsporadicmentalretardation