Associated Papers
Identifying rare genetic variants in 21 highly multiplex autism families: the role of diagnosis and autistic traits.
More RP et al.
Molecular Psychiatry, 2023
Challenges and opportunities in the investigation of unexplained intellectual disability using family-based whole-exome sequencing.
Helsmoortel C et al.
Clinical Genetics, 2015
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1635.580
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