المؤلفون: B. Huber, Sumin Gu, K. Senyi, Barbara Grammatico, Andreas Gal, G. Jojart, A. Veske, G. Del Porto

المصدر: Acta Ophthalmologica Scandinavica. 74:13-16

مصطلحات موضوعية: Male, X Chromosome, Genetic Linkage, Norrie Syndrome, DNA Mutational Analysis, Deafness, Gene mutation, Blindness, Polymerase Chain Reaction, medicine, Humans, Point Mutation, Missense mutation, In patient, Clinical phenotype, X chromosome, Genetics, business.industry, Mental Disorders, DNA, Syndrome, medicine.disease, Phenotype, Pedigree, Ophthalmology, Child, Preschool, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dde74bb870598227f415b87c8de59af5
https://doi.org/10.1111/j.1600-0420.1996.tb00374.x

المؤلفون: M POPPER, M BAUSZ, E TURI, K SENYI, K KNEZY, I SUVEGES

المصدر: Acta Ophthalmologica Scandinavica. 85

مصطلحات موضوعية: Ophthalmology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::108f7a6f61f0031dbbea698c6c141f0b
https://doi.org/10.1111/j.1600-0420.2007.01063_3339.x