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4. Combined CNV, haplotyping and whole exome sequencing enable identification of two distinct novel EYS mutations causing RP in a single inbred tribe. Issue 12 (4th December 2018)

7. Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred. Issue 1 (December 2016)

8. Peripheral Blunt Dissection: Using a Microhoe-Facilitated Method for Descemet Membrane Endothelial Keratoplasty Donor Tissue Preparation. Issue 10 (October 2017)