Cargando…
The psychiatric phenotypes of 1q21 distal deletion and duplication
Copy number variants are amongst the most highly penetrant risk factors for psychopathology and neurodevelopmental deficits, but little information about the detailed clinical phenotype associated with particular variants is available. We present the largest study of the microdeletion and -duplicati...
Autores principales: | Linden, Stefanie C., Watson, Cameron J., Smith, Jacqueline, Chawner, Samuel J. R. A., Lancaster, Thomas M., Evans, Ffion, Williams, Nigel, Skuse, David, Raymond, F. Lucy, Hall, Jeremy, Owen, Michael J., Linden, David E. J., Green-Snyder, LeeAnne, Chung, Wendy K., Maillard, Anne M., Jacquemont, Sébastien, van den Bree, Marianne B. M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862693/ https://www.ncbi.nlm.nih.gov/pubmed/33542195 http://dx.doi.org/10.1038/s41398-021-01226-9 |
Ejemplares similares
-
Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication
por: Linden, Stefanie C., et al.
Publicado: (2021) -
Psychiatric disorders in children with 16p11.2 deletion and duplication
por: Niarchou, Maria, et al.
Publicado: (2019) -
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication
por: Niarchou, Maria, et al.
Publicado: (2019) -
Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology
por: Morrison, Sinead, et al.
Publicado: (2020) -
Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome
por: Chapman, Gareth, et al.
Publicado: (2021)