Sensenbrenner syndrome: a further challenge in evaluating sagittal synostosis and a need for a multidisciplinary approach

Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome

Christian Gilissen, Heleen H. Arts, Alexander Hoischen et al. · The American Journal of Human Genetics · 2010 · 279 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Ciliopathies with Skeletal Anomalies and Renal Insufficiency due to Mutations in the IFT-A Gene WDR19

Cecilie Bredrup, Sophie Saunier, Machteld M. Oud et al. · The American Journal of Human Genetics · 2011 · 237 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene

Joanna Walczak‐Sztulpa, Jonathan Eggenschwiler, Daniel P. S. Osborn et al. · The American Journal of Human Genetics · 2010 · 208 citations · Full text

Medicine, Molecular Medicine, Pathology +11

Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium

José A. Caparrós‐Martín, Alessandro De Luca, François Cartault et al. · Human Molecular Genetics · 2015 · 55 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

New syndrome of skeletal, dental and hair anomalies.

Sensenbrenner Ja, Dorst Jp, Owens Rp · PubMed · 1975 · 44 citations

Medicine, Genetics, Pediatrics +17