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1. Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals

2. Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals

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3. Elucidating the clinical and molecular spectrum ofSMARCC2-associated NDD in a cohort of 65 affected individuals

4. Natural history of KBG syndrome in a large European cohort

6. Natural history of KBG syndrome in a large European cohort

7. New Candidates for Autism/Intellectual Disability Identified by Whole-Exome Sequencing

8. Natural history of KBG syndrome in a large European cohort