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Title

Does differential visual exploration contribute to visual memory impairments in 22q11.2 microdeletion syndrome?
Authors
Bostelmann, Mathilde
Glaser, Bronwyn
Zaharia, Alexandra
Eliez, Stéphan
Schneider, Maude
Published in Journal of Intellectual Disability Research. 2017, vol. 61, no. 12, p. 1174-1184
Abstract Chromosome 22q11.2 microdeletion syndrome (22q11.2DS) is a genetic syndrome characterised by a unique cognitive profile. Individuals with the syndrome present several non-verbal deficits, including visual memory impairments and atypical exploration of visual information. In this study, we seek to understand how visual attention may contribute to memory difficulties in 22q11.2DS by tracking eye movements during the encoding phase of a visual short-term memory task.
Identifiers
PMID: 29154491
Full text
Article (Published version) (406 Kb) - document accessible for UNIGE members only Limited access to UNIGE
Structures
Faculté de médecine / Section de médecine clinique / Département de psychiatrie
Faculté de médecine / Section de médecine fondamentale / Département de médecine génétique et développement
Centres et instituts / Centre interfacultaire des sciences affectives
Research groups Laboratoire d'imagerie et de psychopathologie développementale (693)
Affective sciences
Citation
(ISO format) 		BOSTELMANN, Mathilde et al. Does differential visual exploration contribute to visual memory impairments in 22q11.2 microdeletion syndrome?. In: Journal of Intellectual Disability Research, 2017, vol. 61, n° 12, p. 1174-1184. https://archive-ouverte.unige.ch/unige:102774

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Deposited on : 2018-03-07

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