• Protein Isoforms/genetics [MeSH] [x]
• Phenotype [MeSH] [x]
• Neurodevelopmental Disorders/genetics [MeSH] [x]
• Male [MeSH] [x]
• Loss of Heterozygosity [MeSH] [x]
• Isoform-based phenotypic continuum [x]
• Intellectual disability [x]
• Intellectual Disability/genetics [MeSH] [x]

Sacherschließung

• Original Article (1)
• Mutation, Missense/genetics [MeSH] (1)

Publikationstyp

• Artikel (1)

Erscheinungsjahr

• 2021 (1)

Institution