Associated Papers
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes.
Marianski K et al.
Human Genetics, 2025
41442065 (PubMed )
Supplement: 439_2025_2796_MOESM4_ESM.xlsx › ST2
The genomic complexity of primary human prostate cancer.
Berger MF et al.
Nature, 2011
21307934 (PubMed )
Supplement: NIHMS257464-supplement-2.xlsx › TABLE_S3
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