Utility of trio-based exome sequencing in the elucidation of the genetic basis of isolated syndromic intellectual disability: illustrative cases

INTRODUCTION: Exome sequencing is recognized as a powerful tool for identifying the genetic cause of intellectual disability (ID). It is uncertain, however, whether only the exome of the proband should be sequenced or if the sequencing of parental genomes is also required, and the resulting increase...

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Detalles Bibliográficos
Autores principales: Carneiro, Thaise NR, Krepischi, Ana CV, Costa, Silvia S, Tojal da Silva, Israel, Vianna-Morgante, Angela M, Valieris, Renan, Ezquina, Suzana AM, Bertola, Debora R, Otto, Paulo A, Rosenberg, Carla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110279/
https://www.ncbi.nlm.nih.gov/pubmed/30174453
http://dx.doi.org/10.2147/TACG.S165799

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110279/
https://www.ncbi.nlm.nih.gov/pubmed/30174453
http://dx.doi.org/10.2147/TACG.S165799

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