RINALDI, BERARDO

RINALDI, BERARDO  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
Ocular features in Williams-Beuren syndrome: a review of the literature 2023 Nassisi, MarcoAretti, AndreaSperti, AndreaRinaldi, BerardoViola, Francesco + Article (author) -
Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes 2023 Rinaldi, BerardoMilani, DonatellaGrilli, FedericoMarchisio, Paola + Article (author) -
Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome 2022 Rinaldi, BerardoCesaretti, ClaudiaBorzani, IreneConte, GiorgioCinnante, ClaudiaTriulzi, FabioPersico, Nicola + Article (author) -
Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology 2022 Moresco, GiadaRondinone, OrnellaMauri, AlessiaColapietro, PatriziaMarfia, GiovanniGrilli, FedericoRinaldi, BerardoPrada, ElisabettaMiozzo, Monica RosaMilani, DonatellaFontana, Laura + Article (author) -
Incidental finding of APC deletion in a child: double trouble or double chance? – a case report 2021 Rosina E.Rinaldi B.Silipigni R.Marchisio P. G. + Article (author) -