Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases

PURPOSE: To describe examples of missed pathogenic variants on whole exome sequencing (WES) and the importance of deep phenotyping for further diagnostic testing. METHODS: Guided by phenotypic information, three children with negative WES underwent targeted single gene testing. RESULTS: Individual 1...

Descripción completa

Detalles Bibliográficos
Autores principales: Pena, Loren DM, Jiang, Yong-Hui, Schoch, Kelly, Spillmann, Rebecca C., Walley, Nicole, Stong, Nicholas, Horn, Sarah Rapisardo, Sullivan, Jennifer A., McConkie-Rosell, Allyn, Kansagra, Sujay, Smith, Edward C., El-Dairi, Mays, Bellet, Jane, Ann Keels, Martha, Jasien, Joan, Kranz, Peter G., Noel, Richard, Nagaraj, Shashi K., Lark, Robert K., Wechsler, Daniel SG, del Gaudio, Daniela, Leung, Marco L., Hendon, Laura G., Parker, Collette C., Jones, Kelly L., Goldstein, David B., Shashi, Vandana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851806/
https://www.ncbi.nlm.nih.gov/pubmed/28914269
http://dx.doi.org/10.1038/gim.2017.128

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851806/
https://www.ncbi.nlm.nih.gov/pubmed/28914269
http://dx.doi.org/10.1038/gim.2017.128

Ejemplares similares