P. Cerruti Mainardi

Cri du Chat syndrome

P. Cerruti Mainardi, 2006, Orphanet journal of rare diseases.

Epilepsy in Mowat–Wilson syndrome: Delineation of the electroclinical phenotype

F. Licata, E. Terazzi, S. Savasta, 2013, American journal of medical genetics. Part A.

[Longterm repercussions of splenectomy in childhood. (Clinical and biological study)].

C. Borrone, P. Cerruti Mainardi, 1963, Minerva pediatrica.

Mowat–Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity

A. Rauch, C. Zweier, G. Pastore, 2004, Journal of Medical Genetics.

[A case of maple syrup urine disease].

P. Cerruti Mainardi, 1966, Minerva pediatrica.

Psychomotor development in Cri du Chat Syndrome

A. Guala, G. Pastore, M. Pierluigi, 2000, Clinical genetics.

[The Cri du Chat syndrome: a study on the quality of care].

A. Guala, G. Pastore, C. Castronovo, 2012, Minerva pediatrica.