We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleCiliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3.AuthorsTammachote, Rachaneekorn; Hommerding, Cynthia J.; Sinders, Rachel M.; Miller, Caroline A.; Czarnecki, Peter G.; Leightner, Amanda C.; Salisbury, Jeffrey L.; Ward, Christopher J.; Torres, Vicente E.; Gattone, Vincent H.; Harris, Peter C.PublicationHuman Molecular Genetics, 2009, Vol 18, Issue 17, p3311ISSN0964-6906Publication typearticleDOI10.1093/hmg/ddp272