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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Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: The Association for Research in Vision and Ophthalmology 2014
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Accesso online: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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