Associated Papers
Comprehensive characterization of pathogenic missense CTRP6 variants and their association with cancer.
Mehboob MZ et al.
Bmc Cancer, 2025
39979869 (PubMed )
Supplement: 12885_2025_13685_MOESM2_ESM.xlsx › Table_S1
Rare dentin defects: Understanding the pathophysiological mechanisms of COLXVA1 mutations.
Bugueno IM et al.
Genes & Diseases, 2024
38721411 (PubMed )
Supplement: mmc2.pdf
Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hip.
Dembic M et al.
Molecular Genetics and Genomics : Mgg, 2023
36454308 (PubMed )
Supplement: 438_2022_1980_MOESM4_ESM.xlsx › List_of_genes
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