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Community Eye Exam Project
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Research and gene calculater
The Israeli Consortium for Retinal Disease Research
Members of the Israeli Consortium for Inherited Retinal Diseases
Publications of the Israeli Consortium for Hereditary Retinal Diseases
Consortium Genetically Tests 40 Percent of People in Israel with IRDs
Late diagnosis of Alstrom syndrome in a Yemenite-Jewish child.
[THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES]
A novel intronic mutation of PDE6B is a major cause of autosomal recessive retinitis pigmentosa among Caucasus Jews
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophy.
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)
THE TARGET SIGN: A Near Infrared Feature and Multimodal Imaging in a Pluri-Ethnic Cohort with RDH5-Related Fundus Albipunctatus
Autosomal dominant retinitis pigmentosa with incomplete penetrance due to an intronic mutation of the PRPF31 gene
Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry
Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli Population
Nationwide Prevalence of Inherited Retinal Diseases in the Israeli Population
Retinal Disease Gene Calculator
The Israeli Stem Cell Research Consortium
Winners of research grants from the Lirot Association
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