פרסומי הקונסורציום הישראלי למחלות רשתית תורשתיות

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