Open AccessGenetic Variants Associated With Severe Retinopathy of Prematurity in Extremely Low Birth Weight Infants
Author(s) -
M. Elizabeth Hartnett,
Margaux A. Morrison,
Silvia E. Smith,
Tammy L. Yanovitch,
Terri L. Young,
Tarah T. Colaizy,
Allison M. Momany,
John M. Dagle,
Waldemar A. Carlo,
Erin Clark,
Grier P. Page,
Jeff Murray,
Margaret M. DeAngelis,
C. Michael Cotten
Publication year - 2014
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.14-14841
Subject(s) - retinopathy of prematurity , cohort , single nucleotide polymorphism , medicine , cohort study , candidate gene , pediatrics , genetics , biology , genotype , gestational age , gene , pregnancy
To determine genetic variants associated with severe retinopathy of prematurity (ROP) in a candidate gene cohort study of US preterm infants.
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