The psychosocial impact of 22q11 deletion syndrome on patients and families: A systematic review
Author:
Affiliation:
1. Sheffield Institute of Translational Neuroscience, The University of Sheffield; Sheffield United Kingdom
2. Sheffield Clinical Genetics Service, Sheffield Children's Hospital NHS Foundation Trust, Western Bank; Sheffield United Kingdom
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.38673/fullpdf
Reference62 articles.
1. Australian families living with rare disease: Experiences of diagnosis, health services use and needs for psychosocial support;Anderson;Orphanet Journal of Rare Diseases,2013
2. An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome;Angkustsiri;Journal of Developmental and Behavioral Pediatrics,2012
3. Patient and family experiences and opinions on adding 22q11 deletion syndrome to the newborn screen;Bales;Journal of Genetic Counseling,2010a
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3. Undeleting the voice of people with 22q11 deletion syndrome: A scoping review;Rare;2024
4. Exploring Health Literacy in 22q11.2 Deletion Syndrome: A Comprehensive Study on Access to Information, Teleorientation, and Social Media Engagement in Brazil;2023-12-08
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