Marco Pessina

Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features

L. Persani, V. Cirello, L. Fugazzola, 2018, Front. Genet..

A 2.3 Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected by standard karyotype

R. Borgatti, R. Tenconi, R. Giorda, 2005, European Journal of Human Genetics.

Cerebroretinal Microangiopathy With Calcifications and Cysts Associated With CTC1 and NDP Mutations

R. Borgatti, F. Triulzi, F. Arrigoni, 2013, Journal of child neurology.

Femorally inserted central catheters with exit site at mid-thigh: A low risk alternative for central venous catheterization.

G. Foti, A. Lucchini, S. Elli, 2022, The journal of vascular access.