Associated Papers
Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders.
Li K et al.
Ebiomedicine, 2024
38113761 (PubMed )
Supplement: mmc2.xlsx › Table_S4
Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.
Zhang Y et al.
Molecular Neurobiology, 2021
33860439 (PubMed )
Supplement: 12035_2021_2377_MOESM14_ESM.xlsx › NDD_probands__public_
Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders.
Han L et al.
Molecular Genetics & Genomic Medicine, 2019
31199603 (PubMed )
Supplement: MGG3-7-e00789-s001.xlsx › Table_S1
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