Reanalysis of exome negative patients with rare disease: a pragmatic workflow for diagnostic applications

BACKGROUND: Approximately two third of patients with a rare genetic disease remain undiagnosed after exome sequencing (ES). As part of our post-test counseling procedures, patients without a conclusive diagnosis are advised to recontact their referring clinician to discuss new diagnostic opportuniti...

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Detalles Bibliográficos
Autores principales: Schobers, Gaby, Schieving, Jolanda H., Yntema, Helger G., Pennings, Maartje, Pfundt, Rolph, Derks, Ronny, Hofste, Tom, de Wijs, Ilse, Wieskamp, Nienke, van den Heuvel, Simone, Galbany, Jordi Corominas, Gilissen, Christian, Nelen, Marcel, Brunner, Han G., Kleefstra, Tjitske, Kamsteeg, Erik-Jan, Willemsen, Michèl A. A. P., Vissers, Lisenka E. L. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204949/
https://www.ncbi.nlm.nih.gov/pubmed/35710456
http://dx.doi.org/10.1186/s13073-022-01069-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9204949/
https://www.ncbi.nlm.nih.gov/pubmed/35710456
http://dx.doi.org/10.1186/s13073-022-01069-z

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