Associated Papers
Genetic landscape of human oocyte/embryo defects.
Chen B et al.
Cell Genomics, 2026
41005306 (PubMed )
Supplement: mmc3.xlsx › Table_S2
Human organoids for rapid validation of gene variants linked to cochlear malformations.
Zafeer MF et al.
Human Genetics, 2025
39786576 (PubMed )
Supplement: 439_2024_2723_MOESM1_ESM.docx
Genetic Dissection of Hypertrophic Cardiomyopathy with Myocardial RNA-Seq.
Gao J et al.
International Journal of Molecular Sciences, 2020
Select a paper to view details