One platform for all researcher needs
AI-powered academic writing assistant
Your #1 AI companion for literature search
AI tool for graphics, illustrations, and artwork
Unlock unlimited use of all AI tools with the Editage Plus membership.
Explore Editage Plus
Audio Papers
Ask R Discovery
Translation
Auto-sync
Collaboration
Open Access
PDF Availablehttps://doi.org/10.1136/archdischild-2012-302724.0741
Copy DOI
Export
Save
Share
Cite Journal: Archives of Disease in Childhood |  Publication Date: Oct 1, 2012 |
Affiliation: Hopital Universitaire Hedi Chaker
BackgroundPeters Plus syndrome is an autosomal recessive and rare disorder characterized by a variety of anterior eye chamber defects, of which the Peters anomaly occurs most frequently. Other major symptoms...
Free) Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
