Associated Papers
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Anderson EN et al.
American Journal of Human Genetics, 2026
41468891 (PubMed )
Supplement: mmc1.pdf
Whole-Exome Sequencing Reveals the Genomic Features of the Micropapillary Component in Ground-Glass Opacities.
Meng F et al.
Cancers, 2022
36077702 (PubMed )
Supplement: cancers-14-04165-s001.zip › cancers-1855002-supplementary-for_xml › Table_S3.xlsx › Sheet3
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