Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations

Zaharia, Alexandra; Schneider, Maude; Glaser, Bronwyn; Franchini, Martina; Menghetti, Sarah; Schaer, Marie; Debbané, Martin; Eliez, Stéphan

doi:10.1186/s11689-018-9245-x

Scientific article

Open access

English

Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations

ContributorsZaharia, Alexandra; Schneider, Maude; Glaser, Bronwyn; Franchini, Martina; Menghetti, Sarah; Schaer, Marie; Debbané, Martin; Eliez, Stéphan

Published inJournal of Neurodevelopmental Disorders, vol. 10, no. 26

Publication date2018

Affiliation

Research group

Citation (ISO format)

ZAHARIA, Alexandra et al. Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations. In: Journal of Neurodevelopmental Disorders, 2018, vol. 10, n° 26. doi: 10.1186/s11689-018-9245-x

Article (Published version)

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Identifiers

PID : unige:109266
DOI : 10.1186/s11689-018-9245-x
PMID : 30157749

Commercial URLhttps://jneurodevdisorders.biomedcentral.com/articles/10.1186/s11689-018-9245-x

ISSN of the journal1866-1947

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Creation09/15/2018 12:48:00 PM

First validation09/15/2018 12:48:00 PM

Update time03/15/2023 8:47:05 AM

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Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations

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