Maria Teresa Bonati

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 3

Top Topics

Intellectual Disability

End Stage Renal Disease

Ejection Fraction

Top Venues

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Maria Teresa Bonati, Agnese Feresin, Paolo Prontera, Paola Michieletto, Valeria Gambacorta, Giampietro Ricci, Eva Orzan
Contiguous Gene Syndromes and Hearing Loss: A Clinical Report of Xq21 Deletion and Comprehensive Literature Review. Genes 15 (6) (2024)
Maria Teresa Bonati, Agnese Feresin, Paolo Prontera, Paola Michieletto, Valeria Gambacorta, Giampietro Ricci, Eva Orzan
Contiguous Gene Syndromes and Hearing Loss: A Clinical Report of Xq21 Deletion and Comprehensive Literature Review. Genes 15 (6) (2024)
Luca Ferrari, Eleonora Mangano, Maria Teresa Bonati, Ilaria Monterosso, Daniele Capitanio, Federica Chiappori, Ilaria Brambilla, Cecilia Gelfi, Cristina Battaglia, Roberta Bordoni, Paola Riva
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model? European journal of human genetics : EJHG 28 (10) (2020)