Rute Luísa Cabrita Pinto (Rute Pinto)

Publication Activity (10 Years)

Years Active: 2023-2023
Publications (10 Years): 5

Top Topics

Autism Spectrum Disorder

Intellectual Disability

Top Venues

Journal of personalized medicine

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

Publications

Rute Luísa Cabrita Pinto, Silvia Viaggi, Edoardo Canale, Marina Martinez Popple, Valeria Capra, Giuseppina Conteduca, Barbara Testa, Domenico A Coviello, Angela Elvira Covone
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome. Genes 14 (4) (2023)
Rute Luísa Cabrita Pinto, Silvia Viaggi, Edoardo Canale, Marina Martinez Popple, Valeria Capra, Giuseppina Conteduca, Barbara Testa, Domenico A Coviello, Angela Elvira Covone
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome. Genes 14 (4) (2023)
Rute Luísa Cabrita Pinto, Silvia Viaggi, Edoardo Canale, Marina Martinez Popple, Valeria Capra, Giuseppina Conteduca, Barbara Testa, Domenico A Coviello, Angela Elvira Covone
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome. Genes 14 (4) (2023)
Rute Luísa Cabrita Pinto, Silvia Viaggi, Edoardo Canale, Marina Martinez Popple, Valeria Capra, Giuseppina Conteduca, Barbara Testa, Domenico A Coviello, Angela Elvira Covone
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome. Genes 14 (4) (2023)
José Bragança, Rute Luísa Cabrita Pinto, Bárbara M Silva, Nuno Marques, Helena S Leitão, Mónica T Fernandes
Charting the Path: Navigating Embryonic Development to Potentially Safeguard against Congenital Heart Defects. Journal of personalized medicine 13 (8) (2023)