Associated Papers
Rare damaging variants in the sex differences of congenital heart disease: an exome sequencing study.
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Supplement: mmc2.xlsx › Supplementary_Table_6
Diagnostic Utility of Trio-Exome Sequencing for Children With Neurodevelopmental Disorders.
Lan X et al.
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Supplement: jamanetwopen-e251807-s002.xlsx › eTable4
Molecular subtyping and genomic profiling expand precision medicine in refractory metastatic triple-negative breast cancer: the FUTURE trial.
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Supplement: 41422_2020_375_MOESM12_ESM.xlsx › Sheet1
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