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المؤلفون: Christos Iosifidis, Jingshu Liu, Theodora Gale, Jamie M. Ellingford, Christopher Campbell, Stuart Ingram, Kate Chandler, Neil R. A. Parry, Graeme C. Black, Panagiotis I. Sergouniotis
المصدر: Acta Ophthalmologica. 100
مصطلحات موضوعية: Chromosomes, Human, Pair 15, TRPM Cation Channels, Chromosome Disorders, Eye Diseases, Hereditary, Genetic Diseases, X-Linked, General Medicine, Pedigree, Ophthalmology, Night Blindness, Seizures, Intellectual Disability, Mutation, Electroretinography, Myopia, Humans, Chromosome Deletion
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4c39454a873ee1d305b8b0a9d76cc56Test
https://doi.org/10.1111/aos.15186Test -
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المؤلفون: Panagiotis I. Sergouniotis, Cecilia Fenerty, Graeme C.M. Black, James O'Sullivan, Jamie M Ellingford
المصدر: Acta Ophthalmologica. 95:e249-e250
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, Genotype, Glaucoma, Biology, DNA sequencing, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Pupil Disorders, medicine, Humans, Point Mutation, Genetic Testing, Child, Eye Proteins, Genetics, Chromosomes, Human, Pair 13, General Medicine, Microcoria, medicine.disease, Pedigree, Ophthalmology, 030104 developmental biology, 030221 ophthalmology & optometry, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1577979856176d2044cc6e34b6f25422Test
https://doi.org/10.1111/aos.13246Test