Associated Papers
Novel SRY-box transcription factor 9 variant in campomelic dysplasia and the location of missense and nonsense variants along the protein domains: A case report.
Calvache CA et al.
Frontiers in Pediatrics, 2022
Genetic Mutations Associated with Pierre Robin Syndrome/Sequence: A Systematic Review.
Varadarajan S et al.
Molecular Syndromology, 2021
SOX9 dimerization domain mutation mimicking type 2 collagen disorder phenotype.
Takenouchi T et al.
European Journal of Medical Genetics, 0
Select a paper to view details