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2. Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data. Issue 9 (22nd April 2016)

4. SENIOR–LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular Diagnosis. Issue 10 (October 2021)

5. Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children. Issue 6 (November 2021)