Cargando…
Universal Multi Gene Panel Testing For Individuals With Pheochromocytomas And Paragangliomas
Background: Pheochromocytomas (PCCs) and paragangliomas (PGLs) (PPGLs) are a genetically heterogeneous entity, with roughly 25-40% of cases found to harbor a pathogenic or likely pathogenic germline alteration. Existing practice guidelines advocating for the use of a sequential gene testing strategy...
Autores principales: | Horton, Carolyn, Richardson, Marcy, Durda, Kate, Yussuf, Amal, Jackson, Michelle, Jasperson, Kory, Tian, Yuan, LaDuca, Holly, Else, Tobias |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265875/ http://dx.doi.org/10.1210/jendso/bvab048.1048 |
Ejemplares similares
-
Universal Germline Panel Testing for Individuals With Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield
por: Horton, Carolyn, et al.
Publicado: (2022) -
SUN-710 Custom Panel to Diagnosis Genetic Endocrine Disorders in a Tertiary Academic Hospital
por: Cardoso, Lais Cavalca, et al.
Publicado: (2020) -
The Use of Genetic Testing Panels for Dyslipidemia: A Quality Improvement Project at the McGill University Health Centre
por: Pasqua, Melissa-Rosina, et al.
Publicado: (2021) -
SUN-034 Genetic Diagnosis of Congenital Isolated or Combined Growth Hormone Deficiency by Massive Parallel Sequencing Using a Target Gene Panel
por: NAKAGUMA, MARILENA, et al.
Publicado: (2019) -
Differential Activity and Utilization of Glucocorticoid Receptor Binding Sites Yields Transcriptional Heterogeneity
por: Hoffman, Jackson Andrew, et al.
Publicado: (2021)