Aldo Mari

22q11 deletions in isolated and syndromic patients with tetralogy of Fallot

Francesca Amati, Aldo Mari, MariaCristina Digilio et al. · Human Genetics · 1995 · 124 citations

Down Syndrome, Clinical Disorders, Neurological Disorder +6

Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes

Annalisa Botta, Giuseppe Novelli, Aldo Mari et al. · Journal of Medical Genetics · 1999 · 95 citations · Full text

UFD1L, a Developmentally Expressed Ubiquitination Gene, is Deleted in CATCH 22 Syndrome

Antonio Pizzuti, Giuseppe Novelli, Antonia Ratti et al. · Human Molecular Genetics · 1997 · 87 citations · Full text

Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome

Aldo Mari, Francesca Amati, Rita Mingarelli et al. · Human Genetics · 1995 · 58 citations

Genetic Disorder, Genetics, Pathology +6

Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.

Antonio Pizzuti, Giuseppe Novelli, Aldo Mari et al. · PubMed · 1996 · 47 citations