Associated Papers
Novel compound heterozygous mutation in DNAH9 causes complex congenital heart disease.
Liu X et al.
Molecular Medicine Reports, 2025
40376972 (PubMed )
Supplement: Supplementary_Data2.pdf
Recessive genetic contribution to congenital heart disease in 5,424 probands.
Dong W et al.
Proceedings of the National Academy of Sciences of the United States of America, 2025
40030011 (PubMed )
Supplement: pnas.2419992122.sd02.xlsx › Dataset_S2_-_RGs
Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia.
Tang D et al.
Reproductive Biology and Endocrinology : Rb&e, 2021
Differential Mutation Detection Capability Through Capture-Based Targeted Sequencing in Plasma Samples in Hepatocellular Carcinoma.
Gao J et al.
Frontiers in Oncology, 2021
33996539 (PubMed )
Supplement: DataSheet_8.xlsx › Table_S3
Select a paper to view details