A. Maddalena

DNA topoisomerase II inhibition and gene amplification in V79/B7 cells.

A. Di Leonardo, P. Cavolina, A. Maddalena, 1993, Mutation research.

Nalidixic acid-resistant V79 cells with reduced DNA topoisomerase II activity and amplification prone phenotype.

A. Di Leonardo, P. Cavolina, A. Maddalena, 1992, Mutation research.

Characterization of point mutations in the same arginine codon in three unrelated patients with ornithine transcarbamylase deficiency.

R. Nussbaum, W. O'Brien, J. Spence, 1988, The Journal of clinical investigation.

Prenatal diagnosis and heterozygote detection by DNA analysis in ornithine transcarbamylase deficiency.

A. Beaudet, S. Fernbach, W. O'Brien, 1989, The Journal of pediatrics.

Mosaicism for an intragenic deletion in a boy with mild ornithine transcarbamylase deficiency.

R. Nussbaum, G. Berry, D. Sosnoski, 1988, The New England journal of medicine.

Induction of CAD gene amplification by restriction endonucleases in V79,B7 Chinese hamster cells.

A. Di Leonardo, G. Sciandrello, P. Cavolina, 1989, Mutation research.

Cytogenetic manifestations associated with the reversion, by gene amplification, at the HGPRT locus in V79 Chinese hamster cells.

A. Di Leonardo, G. Sciandrello, P. Cavolina, 1989, Genetical research.