Fabio Corsolini

Prenatal diagnosis of Pelizaeus‐Merzbacher disease: detection of proteolipid protein gene duplication by quantitative fluorescent multiplex PCR

S. Regis, F. Corsolini, M. Filocamo, 2001, Prenatal diagnosis.

Molecular analysis of 40 Italian patients with mucopolysaccharidosis type II: New mutations in the iduronate‐2‐sulfatase (IDS) gene

F. Corsolini, M. Filocamo, R. Cusano, 2001, Human mutation.

Two New Nonsense mutations (Q80X; Q389X) in patients with severe hunter syndrome ( mucopolysaccharidosis type II)

R. Carrozzo, R. Gatti, Fabio Corsolini, 1996, Human mutation.

A deletion involving exons 2–4 in the iduronate‐2‐sulfatase gene of a patient with intermediate Hunter syndrome

S. Regis, F. Corsolini, M. Filocamo, 1998, Clinical genetics.

A T > C transition causing a Leu > Pro substitution in a conserved region of the arylsulfatase A gene in a late infantile metachromatic leukodystrophy patient

S. Regis, M. Filocamo, R. Gatti, 1997, Clinical genetics.