Mundlos, Stefan Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society;
Brunetti-Pierri, N., del Gaudio, D., Peters, H., Justino, H., Ott, C.-E., Mundlos, S., et al. (2008). Robinow syndrome: Phenotypic variability in a family with a novel intragenic ROR2 mutation. American Journal of Medical Genetics Part A, 146A(21), 2804-2809. doi:10.1002/ajmg.a.32530.