| dc.contributor.author | Parisi, Melissa A. | |
| dc.contributor.author | Doherty, Daniel | |
| dc.contributor.author | Arts, Heleen H. | |
| dc.contributor.author | Gorden, Nicholas T. | |
| dc.contributor.author | Eckert, Melissa L. | |
| dc.contributor.author | Shaw, Dennis W. W. | |
| dc.contributor.author | Glass, Ian A. | |
| dc.date.accessioned | 2020-06-21T15:18:31Z | |
| dc.date.available | 2020-06-21T15:18:31Z | |
| dc.date.issued | 2007 | |
| dc.identifier.issn | 0364-5134 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/19700 | |
| dc.description | 132nd Annual Meeting of the American-Neurological-Association -- OCT 07-10, 2007 -- Washington, DC | en_US |
| dc.description | Roepman, Ronald/0000-0002-5178-8163; Dobyns, William/0000-0002-7681-2844 | en_US |
| dc.description | WOS: 000251383300035 | en_US |
| dc.description.abstract | … | en_US |
| dc.description.sponsorship | Amer Neurol Assoc | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Wiley-Liss | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | Spectrum of phenotypic findings in individuals with Joubert syndrome and clinical correlation with identified mutations in the NPHP1,AHI1, and RPGRIP1L genes | en_US |
| dc.type | conferenceObject | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 62 | en_US |
| dc.identifier.issue | 5 | en_US |
| dc.identifier.startpage | 537 | en_US |
| dc.identifier.endpage | 538 | en_US |
| dc.relation.journal | Annals of Neurology | en_US |
| dc.relation.publicationcategory | Konferans Öğesi - Uluslararası - Kurum Öğretim Elemanı | en_US |
