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Endothelial nitric oxide synthase gene T-786C and 27-bp repeat gene polymorphisms in retinopathy of prematurity

Rusai, K; Vannay, A; Szebeni, B; Borgulya, G; Fekete, A; Vásárhelyi, B; Tulassay, T; Szabó, AJ (2008) Endothelial nitric oxide synthase gene T-786C and 27-bp repeat gene polymorphisms in retinopathy of prematurity. MOLECULAR VISION, 14 (34-35). 286 - 290 (5). ISSN 1090-0535
SGUL Authors: Borgulya, Gabor

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Item Type: Article
Additional Information: PubMed ID: 18334945
Keywords: Alleles, Base Pairing, Birth Weight, Cytosine, Female, Gestational Age, Haplotypes, Humans, Infant, Newborn, Male, Nitric Oxide Synthase Type III, Polymerase Chain Reaction, Polymorphism, Genetic, Regression Analysis, Repetitive Sequences, Nucleic Acid, Retinopathy of Prematurity, Thymine, Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, Ophthalmology, SEVERE DIABETIC-RETINOPATHY, OXYGEN-INDUCED RETINOPATHY, ANGIOGENESIS, ASSOCIATION, RISK
Journal or Publication Title: MOLECULAR VISION
ISSN: 1090-0535
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Dates:
DateEvent
5 February 2008Published
Web of Science ID: WOS:000256637300002
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URI: https://openaccess.sgul.ac.uk/id/eprint/1594

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