Prospective and detailed behavioral phenotyping in DDX3X syndrome

BACKGROUND: DDX3X syndrome is a recently identified genetic disorder that accounts for 1–3% of cases of unexplained developmental delay and/or intellectual disability (ID) in females, and is associated with motor and language delays, and autism spectrum disorder (ASD). To date, the published phenoty...

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Detalles Bibliográficos
Autores principales: Tang, Lara, Levy, Tess, Guillory, Sylvia, Halpern, Danielle, Zweifach, Jessica, Giserman-Kiss, Ivy, Foss-Feig, Jennifer H., Frank, Yitzchak, Lozano, Reymundo, Belani, Puneet, Layton, Christina, Lerman, Bonnie, Frowner, Emanuel, Breen, Michael S., De Rubeis, Silvia, Kostic, Ana, Kolevzon, Alexander, Buxbaum, Joseph D., Siper, Paige M., Grice, Dorothy E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127248/
https://www.ncbi.nlm.nih.gov/pubmed/33993884
http://dx.doi.org/10.1186/s13229-021-00431-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127248/
https://www.ncbi.nlm.nih.gov/pubmed/33993884
http://dx.doi.org/10.1186/s13229-021-00431-z

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