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Defining language disorders in children and adolescents with Noonan Syndrome
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 alteration o...
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| Udgivet i: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
John Wiley and Sons Inc.
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7196479/ https://ncbi.nlm.nih.gov/pubmed/32059087 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1069 |
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