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1
المؤلفون: Samer, Khateb, Aya, Shemesh, Ashly, Offenheim, Ruth, Sheffer, Tamar, Ben-Yosef, Itay, Chowers, Rina, Leibu, Britta, Baumann, Bernd, Wissinger, Susanne, Kohl, Eyal, Banin, Dror, Sharon
المصدر: Molecular vision. 28
مصطلحات موضوعية: Phenotype, Haplotypes, Electroretinography, Myopia, Humans, Color Vision Defects, Cone Opsins, Pedigree
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::13a003b4b140e74a4e4fa2a8584ad828Test
https://pubmed.ncbi.nlm.nih.gov/35400991Test -
2
المؤلفون: Prasanthi, Namburi, Samer, Khateb, Segev, Meyer, Tom, Bentovim, Rinki, Ratnapriya, Alisa, Khramushin, Anand, Swaroop, Ora, Schueler-Furman, Eyal, Banin, Dror, Sharon
المصدر: Molecular Vision
مصطلحات موضوعية: Adult, Heterozygote, Georgia, Genotype, Color Vision Defects, Retinal Dystrophies, Exome Sequencing, Electroretinography, Humans, Genetic Testing, Fluorescein Angiography, Child, Phylogeny, Sequence Deletion, Aged, 80 and over, Corneal Dystrophies, Hereditary, Histone-Lysine N-Methyltransferase, Middle Aged, eye diseases, Pedigree, Electrooculography, Phenotype, Complement Factor H, Jews, Female, Tomography, Optical Coherence, Transcription Factors, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::1a358d9afc956ed9a446477c85acc510Test
https://pubmed.ncbi.nlm.nih.gov/32476814Test