Associated Papers
Population-specific putative causal variants shape quantitative traits.
Koyama S et al.
Nature Genetics, 2024
39363016 (PubMed )
Supplement: 41588_2024_1913_MOESM3_ESM.xlsx › ST8_Missense_PPI___0.1
TBX6 as a cause of a combined skeletal-kidney dysplasia syndrome.
Li G et al.
American Journal of Medical Genetics. Part A, 2022
Spondylocostal dysplasia and brachydactyly associated with TBX6 and IHH variants: A case report.
Puvabanditsin S et al.
Clinical Case Reports, 2022
Characterizing rare and low-frequency height-associated variants in the Japanese population.
Akiyama M et al.
Nature Communications, 2019
Select a paper to view details