Gagliardi, Chiara

Disruption of the ProSAP2 Gene in a t(12;22)(q24.1;q13.3) Is Associated with the 22q13.3 Deletion Syndrome

Bonaglia, M. C., Giorda, R., Borgatti, R., Felisari, G., Gagliardi, C., Selicorni, A., & Zuffardi, O. (2001) · The American Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

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Facial expression recognition in Williams syndrome

Gagliardi, C., Frigerio, E., Burt, D. M., Cazzaniga, I., Perrett, D. I., & Borgatti, R. (2003) · Neuropsychologia

Williams Syndrome ResearchFace Recognition and Perception

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