Defining language disorders in children and adolescents with Noonan Syndrome

Abstract Background Noonan Syndrome is a developmental disorder characterized by a distinctive phenotype including facial dysmorphism, webbed neck, short stature, heart defects, and variable cognitive deficits as major features. Over the years, neuropsychological and behavioral studies explored alte...

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Detaylı Bibliyografya
Asıl Yazarlar: Giulia Lazzaro, Cristina Caciolo, Deny Menghini, Francesca Cumbo, Maria C. Digilio, Rossella Capolino, Giuseppe Zampino, Marco Tartaglia, Stefano Vicari, Paolo Alfieri
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Wiley 2020-04-01
Seri Bilgileri:Molecular Genetics & Genomic Medicine
Konular:
IQ
Linguistic functioning
PTPN11
RASopathies
SLI
Online Erişim:https://doi.org/10.1002/mgg3.1069
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