Associated Papers
The pharmacogenomic landscape in the Chinese: An analytics of pharmacogenetic variants in 206,640 individuals.
Wang LY et al.
Innovation (cambridge (mass.)), 2025
39991480 (PubMed )
Supplement: mmc5.xlsx › Sheet1
Genetic and functional analysis of TUBB1 variants in congenital hypothyroidism.
Wang F et al.
Endokrynologia Polska, 2025
Clinical and Molecular Characteristics of Megakaryocytes in Myelodysplastic Syndrome.
Luo F et al.
Global Medical Genetics, 2024
Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.
Chen X et al.
Bmc Medical Genetics, 2019
31146700 (PubMed )
Supplement: 12881_2019_813_MOESM1_ESM.xls › CHD7_ChenXiang_query_Report_Fil
Structural impact of pathogenic SNPs on β-tubulin using molecular dynamics study.
Mansoor Hussain UH et al.
Journal of Biomolecular Structure & Dynamics, 0
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