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pro vyhledávání: '"Jessica Petrilli"'
Autor:
Maria Novelli, Valeria Mammarella, Francesca Calandriello, Sara Temofonte, Marina Goldoni, Ilaria Macchiarulo, Paolo Versacci, Antonio Pizzuti, Jessica Petrilli, Carlo Di Brina, Barbara Caravale
Publikováno v:
Global Pediatrics, Vol 9, Iss , Pp 100179- (2024)
Objective: UPD(16)mat is a rare genetic condition characterized by intrauterine growth deficiency and multiple congenital malformations. To the best of our knowledge, neurodevelopmental disorders have never been described in association with UPD(16)m
Externí odkaz:
https://doaj.org/article/f47c47c4352a428688d23e8224e897d7
