Associated Papers
Familial exudative vitreoretinopathy (FEVR) in a child with novel microarray-defined deletion of 11q14 previously diagnosed as retinopathy of prematurity (ROP).
López-Cañizares A et al.
Ophthalmic Genetics, 2023
Novel FZD4 and LRP5 mutations in a small cohort of patients with familial exudative vitreoretinopathy (FEVR).
Carrera W et al.
Ophthalmic Genetics, 2021
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