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        • 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
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The Israeli Consortium for Retinal Disease Research
The Israeli Stem Cell Research Consortium
Igniting a Medical Revolution Consortium Manager
Winners of research grants from the Lirot Association
Below is a list of past winners of research grants and scholarships awarded by the Lirot Association over the years:

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