Author:
Chen Jiang,Laclef Christine,Moncayo Alejandra,Snedecor Elizabeth R.,Yang Ning,Li Li,Takemaru Ken-Ichi,Paus Ralf,Schneider-Maunoury Sylvie,Clark Richard A.
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference53 articles.
1. Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel-Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects;Abdelhamed;Hum Mol Genet,2013
2. Cranioectodermal dysplasia;Arts,2013
3. Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome;Arts;Nat Genet,2007
4. Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies;Ashe;Hum Mol Genet,2012
5. Ellis-van Creveld syndrome: dental, clinical, genetic and dermatoglyphic findings of a case;Atasu;J Clin Pediatr Dent,2000
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