Giglio, Sabrina

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome

Bonaglia, M. C., Giorda, R., Beri, S., De Agostini, C., Novara, F., Fichera, M., Grillo, L., Galesi, O., Vetro, A., Ciccone, R., et al. (2011) · PLoS Genetics

Genomic variations and chromosomal abnormalitiesDNA Repair Mechanisms

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Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching

Banfi, S., Borsani, G., Rossi, E., Bernard, L., Guffanti, A., Rubboli, F., Marchitiello, A., Giglio, S., Coluccia, E., Zollo, M., et al. (1996) · Nature Genetics

Genomics and Phylogenetic StudiesBioinformatics and Genomic Networks

Cited by 189

Clinical and genetic study of a family with a paternally inherited 15q11–q13 duplication

Marini, C., Cecconi, A., Contini, E., Pantaleo, M., Metitieri, T., Guarducci, S., Giglio, S., Guerrini, R., & Genuardi, M. (2013) · American Journal of Medical Genetics Part A

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 26