Associated Papers
Pathogenic DVL frameshifting variants in Robinow syndrome disrupt WNT signaling and cellular dynamics.
Zhang C et al.
Biorxiv : the Preprint Server for Biology, 2025
Characterization of the Robinow syndrome skeletal phenotype, bone micro-architecture, and genotype-phenotype correlations with the osteosclerotic form.
Shayota BJ et al.
American Journal of Medical Genetics. Part A, 2020
WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome.
White JJ et al.
American Journal of Human Genetics, 2018
Select a paper to view details