Alessandra Pansa

Autism spectrum disorder and intellectual disability in an inherited 2q14.3 micro‐deletion involving CNTNAP5

D. Milani, S. Guerneri, P. Marchisio, 2020, American journal of medical genetics. Part A.

Double homozygosity in CEP57 and DYNC2H1 genes detected by WES: Composite or expanded phenotype?

L. Galletti, L. Pezzani, M. Iascone, 2020, Molecular genetics & genomic medicine.

ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men.

M. Miozzo, S. Sirchia, S. Tabano, 2014, Human reproduction.

Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?

M. Delledonne, T. Liehr, O. Zuffardi, 2018, Molecular genetics & genomic medicine.

Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

C. Augello, F. Lalatta, A. Selicorni, 2013, Epigenetics.