Genetic Variants Associated With Severe Retinopathy of Prematurity in Extremely Low Birth Weight Infants

PURPOSE. To determine genetic variants associated with severe retinopathy of prematurity (ROP) in a candidate gene cohort study of US preterm infants. METHODS. Preterm infants in the discovery cohort were enrolled through the Eunice Kennedy Shriver National Institute of Child Health and Human Develo...

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Detalhes bibliográficos
Main Authors: Hartnett, M. Elizabeth, Morrison, Margaux A., Smith, Silvia, Yanovitch, Tammy L., Young, Terri L., Colaizy, Tarah, Momany, Allison, Dagle, John, Carlo, Waldemar A., Clark, Erin A. S., Page, Grier, Murray, Jeff, DeAngelis, Margaret M., Cotten, C. Michael
Formato: Artigo
Idioma:Inglês
Publicado em: The Association for Research in Vision and Ophthalmology 2014
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4188045/
https://ncbi.nlm.nih.gov/pubmed/25118269
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.14-14841
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