Deep psychophysiological phenotyping of adolescents and adults with 22q11.2 deletion syndrome: a multilevel approach to defining core disease processes

BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is the most common chromosomal interstitial-deletion disorder, occurring in approximately 1 in 2000 to 6000 live births. Affected individuals exhibit variable clinical phenotypes that can include velopharyngeal anomalies, heart defects, T-cell-relate...

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Detalles Bibliográficos
Autores principales: Parker, David A., Cubells, Joseph F., Imes, Sid L., Ruban, Gabrielle A., Henshey, Brett T., Massa, Nicholas M., Walker, Elaine F., Duncan, Erica J., Ousley, Opal Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Study Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262114/
https://www.ncbi.nlm.nih.gov/pubmed/37312091
http://dx.doi.org/10.1186/s12888-023-04888-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262114/
https://www.ncbi.nlm.nih.gov/pubmed/37312091
http://dx.doi.org/10.1186/s12888-023-04888-5

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