Cecconi, Antonella
Ospedale Santa Maria Annunziata
2 papers on CoChat
Most cited papers
- Verified
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
Cited by 224
- Verified
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
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