Associated Papers
Estimating the frequency of causal genetic variants in foetuses with congenital heart defects: a Chinese cohort study.
Lu F et al.
Orphanet Journal of Rare Diseases, 2022
Canine osteosarcoma genome sequencing identifies recurrent mutations in DMD and the histone methyltransferase gene SETD2.
Gardner HL et al.
Communications Biology, 2019
31341965 (PubMed )
Supplement: 42003_2019_487_MOESM10_ESM.xlsx › Primary_Tumor
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