An online survey to understand the needs of caregivers of family members with 22q11 deletion syndrome

T. Cosman, A. Finless, A. L. Rideout, P. Lingley-Pottie, L. D. Palmer, A. Shugar, D. M. McDonald-McGinn, A. Swillen, P. J. McGrath, A. S. Bassett, C. Cytrynbaum, M. Orr, S. Meier

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)
Original languageEnglish
Pages (from-to)860-868
Number of pages9
JournalJournal of Intellectual Disability Research
Volume67
Issue number9
DOIs
Publication statusPublished - Sept 2023
Externally publishedYes

ASJC Scopus Subject Areas

  • Rehabilitation
  • Arts and Humanities (miscellaneous)
  • Neurology
  • Clinical Neurology
  • Psychiatry and Mental health

Keywords

  • caregivers
  • DiGeorge syndrome
  • online intervention
  • psychosocial wellbeing
  • survey

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Cosman, T., Finless, A., Rideout, A. L., Lingley-Pottie, P., Palmer, L. D., Shugar, A., McDonald-McGinn, D. M., Swillen, A., McGrath, P. J., Bassett, A. S., Cytrynbaum, C., Orr, M., & Meier, S. (2023). An online survey to understand the needs of caregivers of family members with 22q11 deletion syndrome. Journal of Intellectual Disability Research, 67(9), 860-868. https://doi.org/10.1111/jir.13061