Disruption of imprinting caused by deletion of the H19 gene region in micePhilip A. Leighton, Shirley M. Tilghman, Robert S. Ingram et al.|Nature|1995Cited by 759
Mouse Mutants Lacking the Type 2 IGF Receptor (IGF2R) Are Rescued from Perinatal Lethality inIgf2andIgf1rNull BackgroundsThomas Ludwig, Argiris Efstratiadis, Marsha L. Davenport et al.|Developmental Biology|1996Cited by 476
Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 GeneJoanna Walczak‐Sztulpa, Andreas W. Kuß, Raoul C. M. Hennekam et al.|The American Journal of Human Genetics|2010Cited by 208
Cell Cycle-Related Kinase (CCRK) regulates ciliogenesis and Hedgehog signaling in miceAshley Snouffer, Jonathan Eggenschwiler|PLoS Genetics|2017Cited by 49