R. Blandino

Genotype‐cardiac phenotype correlations in a large single‐center cohort of patients affected by RASopathies: Clinical implications and literature review

M. Tartaglia, C. Leoni, G. Zampino, 2021, American journal of medical genetics. Part A.

RASopathies and sigmoid-shaped ventricular septum morphology: evidence of a previously unappreciated cardiac phenotype

M. Tartaglia, C. Leoni, G. Zampino, 2022, Pediatric Research.

The heart in RASopathies

B. Gelb, G. Limongelli, J. Kaski, 2022, American journal of medical genetics. Part C, Seminars in medical genetics.

Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review

M. Digilio, C. Leoni, G. Zampino, 2023, Genes.

Smith–Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature

M. Digilio, C. Leoni, G. Zampino, 2021, American journal of medical genetics. Part A.

Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness

M. Digilio, M. Tartaglia, G. Merla, 2023, Clinical genetics.

RASopathies and sigmoid-shaped ventricular septum morphology: evidence of a previously unappreciated cardiac phenotype

M. Tartaglia, C. Leoni, G. Zampino, 2022, Pediatric Research.

Smith Magenis syndrome: First case of congenital heart defect in a patient with Rai1 mutation

C. Leoni, G. Zampino, M. Zollino, 2022, American journal of medical genetics. Part A.