M. Roberti

Masked complex chromosome rearrangement in a child thought to have del(8qter) as the sole cytogenetic abnormality

R. Capolino, C. Surace, M. Digilio, 2008, Cytogenetic and Genome Research.

Mild ring 17 syndrome shares common phenotypic features irrespective of the chromosomal breakpoints location

R. Capolino, C. Surace, M. Digilio, 2009, Clinical genetics.

Syndromic non‐compaction of the left ventricle: associated chromosomal anomalies

B. Marino, M. Digilio, B. Dallapiccola, 2013, Clinical genetics.

Hypoplastic left heart syndrome and 21q22.3 deletion

B. Dallapiccola, R. Capolino, B. Marino, 2015, American journal of medical genetics. Part A.