Publication: Quantitative Phenotype Morbidity Description of SATB2 - Associated Syndrome
Gestores bibliográficos
item.contributor.advisor
ORCID:
Journal Title
Journal ISSN
Volume Title
Publisher
item.page.isbn
item.page.issn
item.page.issne
item.page.doiurl
item.page.extent
item.page.accessRights
Acceso Abierto
item.page.other
item.page.references
Abstract
Characterized by developmental delay with severe speech delay, dental anomalies, cleft palate, skeletal abnormalities, and behavioral difficulties, SATB2-associated syndrome (SAS) is caused by pathoge...
Description
item.page.coverage.spatial
item.page.sponsorship
Citation
Zarate, Y. A., Bosanko, K., Kannan, A., Thomason, A., Nutt, B., Kumar, N., Simmons, K., Hiegert, A., Hartzell, L., Johnson, A., Prater, T., Pérez-Palma, E., Brünger, T., Stefanski, A., Lal, D., & Caffrey, A. R. (2023). Quantitative Phenotype Morbidity Description of SATB2-Associated Syndrome. Human Mutation, 2023, 1–9. https://doi.org/10.1155/2023/8200176
Keywords
item.page.dc.rights
item.page.dc.rights.url
Estadísticas de uso
1 0,8 0,5 0,3 0
Septiembre 2025Octubre 2025Noviembre 2025Diciembre 2025Enero 2026Febrero 2026Marzo 2026