C. Bonaglia

The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.

G. Gimelli, G. Floridia, O. Zuffardi, 1996, American journal of human genetics.

Genetic Correction of Human Induced Pluripotent Stem Cells from Patients with Spinal Muscular Atrophy

S. Salani, C. Donadoni, F. Rizzo, 2012, Science Translational Medicine.

Patients with Spinal Muscular Atrophy Genetic Correction of Human Induced Pluripotent Stem Cells from

S. Salani, C. Donadoni, F. Rizzo, 2012 .

A prenatal case with multiple supernumerary markers identified as derivatives of chromosomes 13, 15, and 20: molecular cytogenetic characterization and review of the literature

A. Orsini, D. Peroni, V. Bertini, 2019, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion

R. Cerini, R. Guerrini, O. Zuffardi, 2008, European Journal of Human Genetics.

Electroclinical pattern in MECP 2 duplication syndrome : Eight new reported cases and review of literature

R. Borgatti, A. Vignoli, C. Zucca, 2015 .

Electroclinical pattern in MECP2 duplication syndrome: Eight new reported cases and review of literature

R. Borgatti, A. Vignoli, C. Zucca, 2012, Epilepsia.

Ring chromosome 9: An atypical case

S. Landolfo, P. Veggiotti, E. Fazzi, 1996, Brain and Development.