RUNX2‐related metaphyseal dysplasia with maxillary hypoplasia: A rare skeletal disorder resembling SFRP4‐related Pyle disease
Article in Clinical Genetics (December 2023)
The most recent citing publications are shown below. View all 8 publications that cite this research output on Dimensions.
Sfrp4 is required to maintain Ctsk-lineage periosteal stem cell niche function
Article in Proceedings of the National Academy of Sciences of the United States of America (November 2023)
A genotype–phenotype correlation in split-hand/foot malformation type 1: further refinement of the phenotypic subregions within the 7q21.3 locus
Article in Frontiers in Molecular Biosciences (October 2023)