Associated Papers
Rare damaging variants in the sex differences of congenital heart disease: an exome sequencing study.
Sun H et al.
Ebiomedicine, 2025
40347836 (PubMed )
Supplement: mmc2.xlsx › Supplementary_Table_6
Case Report: Whole-Exome Sequencing-Based Copy Number Variation Analysis Identified a Novel DRC1 Homozygous Exon Deletion in a Patient With Primary Ciliary Dyskinesia.
Liu Y et al.
Frontiers in Genetics, 2022
35873463 (PubMed )
Supplement: Table1.XLSX › Sheet2
Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes.
Chen S et al.
Human Molecular Genetics, 2020
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