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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...
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. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
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 |
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