Position effects of 22q13 rearrangements on candidate genes in Phelan-McDermid syndrome.
Phelan-McDermid syndrome (PMS) is a multi-system disorder characterized by significant variability in clinical presentation. The genetic etiology is also variable with differing sizes of deletions in the chromosome 22q13 region and types of genetic abnormalities (e.g., terminal or interstitial delet...
Guardado en:
Autores principales: | Sujata Srikanth, Lavanya Jain, Cinthya Zepeda-Mendoza, Lauren Cascio, Kelly Jones, Rini Pauly, Barb DuPont, Curtis Rogers, Sara Sarasua, Katy Phelan, Cynthia Morton, Luigi Boccuto |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/f1e267b546f04ca790d99f80fd77785b |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Parent-reported measure of repetitive behavior in Phelan-McDermid syndrome
por: Siddharth Srivastava, et al.
Publicado: (2021) -
Phelan-McDermid syndrome in two adult brothers: atypical bipolar disorder as its psychopathological phenotype?
por: Verhoeven WMA, et al.
Publicado: (2012) -
Social visual attentional engagement and memory in Phelan-McDermid syndrome and autism spectrum disorder: a pilot eye tracking study
por: Sylvia B. Guillory, et al.
Publicado: (2021) -
Homer1a regulates Shank3 expression and underlies behavioral vulnerability to stress in a model of Phelan-McDermid syndrome
por: Raozhou Lin, et al.
Publicado: (2021) -
A new test for autism spectrum disorder: Metabolic data from different cell types
por: Sujata Srikanth, et al.
Publicado: (2021)