Clinical evaluation of patients with a neuropsychiatric risk copy number variant

Several copy number variants (CNVs) have been identified to confer high risk for a range of neuropsychiatric conditions. Because of advances in genetic testing within clinical settings, patients are increasingly receiving diagnoses of copy number variant genomic disorders. However, clinical guidelin...

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Detalles Bibliográficos
Autores principales: Chawner, Samuel JRA, Watson, Cameron J, Owen, Michael J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219523/
https://www.ncbi.nlm.nih.gov/pubmed/33461126
http://dx.doi.org/10.1016/j.gde.2020.12.012

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219523/
https://www.ncbi.nlm.nih.gov/pubmed/33461126
http://dx.doi.org/10.1016/j.gde.2020.12.012

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