Experiences and concerns of parents of children with a 16p11.2 deletion or duplication diagnosis: a reflexive thematic analysis

Abstract Background 16p11.2 proximal deletion and duplication syndromes (Break points 4–5) (593KB, Chr16; 29.6-30.2mb - HG38) are observed to have highly varied phenotypes, with a known propensity for lifelong psychiatric problems. This study aimed to contribute to a research gap by qualitatively ex...

Description complète

Détails bibliographiques

Auteurs principaux:	Charlotte E. Butter, Caitlin L. Goldie, Jessica H. Hall, Kathy Leadbitter, Emma M.M. Burkitt, Marianne B.M. van den Bree, Jonathan M. Green
Format:	Artigo
Langue:	Inglês
Publié:	BMC 2024-03-01
Collection:	BMC Psychology
Sujets:	16p11.2 deletion 16p11.2 duplication Qualitative Children Families Neurodevelopmental
Accès en ligne:	https://doi.org/10.1186/s40359-024-01609-9
Tags:	Ajouter un tag Pas de tags, Soyez le premier à ajouter un tag!