Aldo Giannotti

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.

J. Korenberg, G. Gimelli, M. Digilio, 2000, Circulation.

Determination of a new collagen type I alpha 2 gene point mutation which causes a Gly640 Cys substitution in osteogenesis imperfecta and prenatal diagnosis by DNA hybridisation.

P. Pignatti, M. Digilio, A. Giannotti, 1994, Journal of medical genetics.

Nonrandom association of atrioventricular canal and del (8p) syndrome.

B. Marino, M. Digilio, A. Giannotti, 1992, American journal of medical genetics.

Genetic heterogeneity of isolated noncompaction of the left ventricular myocardium.

M. Digilio, A. Giannotti, B. Dallapiccola, 1999, American journal of medical genetics.

Clinical and cardiorespiratory assessment in children with Down syndrome without congenital heart disease.

E. Pastore, B. Marino, A. Calzolari, 2000, Archives of pediatrics & adolescent medicine.

Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome).

M. Digilio, A. Giannotti, B. Dallapiccola, 1999, British journal of audiology.