"Neurodevelopmental outcome of a child with UPD(16)mat: A case report"

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)mat, nor a comprehensive neuropsychological profile...

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Main Authors: Maria Novelli (Author), Valeria Mammarella (Author), Francesca Calandriello (Author), Sara Temofonte (Author), Marina Goldoni (Author), Ilaria Macchiarulo (Author), Paolo Versacci (Author), Antonio Pizzuti (Author), Jessica Petrilli (Author), Carlo Di Brina (Author), Barbara Caravale (Author)
Format: Book
Published: Elsevier, 2024-09-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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