Published in
Wiley Open Access, Clinical Case Reports, 1(9), p. 314-321, 2020
DOI: 10.1002/ccr3.3523
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Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature review
Journal article published in 2020 by
Aurora Arghir 
,
Sorina Mihaela Papuc,
Andreea‐Cristina Tutulan‐Cunita,
Alina Erbescu,
Sara Loddo,
Silvia Genovese,
Laura Ciocca,
Marina Goldoni ,
Carmelo Piscopo,
Laura Bernardini ,
Antonio Novelli,
Magdalena Budisteanu
,
Sorina Mihaela Papuc,
Andreea‐Cristina Tutulan‐Cunita,
Alina Erbescu,
Sara Loddo,
Silvia Genovese,
Laura Ciocca,
Marina Goldoni ,
Carmelo Piscopo,
Laura Bernardini ,
Antonio Novelli,
Magdalena Budisteanu
This paper is made freely available by the publisher.
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