Elena Banaudi

Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study

M. Digilio, B. Dallapiccola, M. Tartaglia, 2020, Birth defects research.

Prenatal features of Noonan syndrome: prevalence and prognostic value

M. Tartaglia, G. Ferrero, M. Silengo, 2011, Prenatal diagnosis.

Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results.

M. Digilio, B. Dallapiccola, M. Tartaglia, 2017, International journal of cardiology.

ECG in noonan syndrome: beyond the "normal abnormalities".

G. Ferrero, G. Baldassarre, G. Agnoletti, 2019, Minerva Cardioangiologica : a Journal on Cardiovascular Pathophysiology, Clinical Medicine and Therapy.

Presenting phenotype and clinical evaluation in a cohort of 22 Williams-Beuren syndrome patients.

L. Peruzzi, G. Ferrero, L. D. di Cantogno, 2007, European journal of medical genetics.

Phenotypic variability associated with the invariant SHOC2 c.4A>G (p.Ser2Gly) missense mutation

M. Tartaglia, G. Ferrero, M. Silengo, 2014, American journal of medical genetics. Part A.

Complete Transposition of the Great Arteries: Patterns of Congenital Heart Disease in Familial Precurrence

M. Digilio, A. Giannotti, B. Dallapiccola, 2001, Circulation.

Clinical and molecular characterization of 40 patients with Noonan syndrome.

G. Ferrero, M. Silengo, E. Biamino, 2008, European journal of medical genetics.

Familial recurrence of transposition of the great arteries

M. Digilio, B. Dallapiccola, B. Marino, 1998, The Lancet.

Data on cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results

M. Digilio, B. Dallapiccola, M. Tartaglia, 2017, Data in brief.