CORE
🇺🇦
make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Filters
1 research outputs found
Spectrum of phenotypic findings in individuals with Joubert syndrome and clinical correlation with identified mutations in the NPHP1,AHI1, and RPGRIP1L genes
Author
Al Swaid Abdulrahman
Arts Heleen H.
+17 more
Bakhsh Eman
Bennett Craig L.
Chance Phillip F.
Dobyns William B.
Dohayan Noura
Doherty Daniel
Eckert Melissa L.
Giray Ozlem
Glass Ian A.
Gorden Nicholas T.
Indridason Olafur S.
Knoers Nine V. A. M.
Ozyurek Hamit
Parisi Melissa A.
Roepman Ronald
Shahwan Saad Al
Shaw Dennis W. W.
Publication venue
Publication date
01/11/2007
Field of study
No full text
Dokuz Eylul University Research Information System