Search Results - "Noureldine, Jinane"

Genotype-phenotype associations in CRB1 bi-allelic patients: a novel mutation, a systematic review and meta-analysis by Daher, Ahmad, Banjak, Malak, Noureldine, Jinane, Nehme, Joseph, El Shamieh, Said

“…The goal of the study was to search for novel bi-allelic CRB1 mutations, and then to analyze the CRB1 literature at the genotypic and phenotypic levels. We…”
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The genetic landscape of inherited retinal dystrophies in Arabs by Jaffal, Lama, Joumaa, Hawraa, Noureldine, Jinane, Banjak, Malak, Ibrahim, Mariam, Mrad, Zamzam, Salami, Ali, Shamieh, Said El

“…Inherited retinal dystrophies (IRDs) are a major cause of vision loss. Altogether are highly heterogeneous genotypically and phenotypically, exhibiting…”
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