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Presence of the R1748X mutation in the NF1 gene in a Brazilian patient with ectropion uveae
(Karger, 2004-01-01)
Congenital ectropion uveae is a rare, nonprogressive anomaly characterized by the presence of iris pigment epithelium on the anterior surface of the iris stroma and is occasionally associated with Rieger's anomaly, ...
Presence of the R1748X mutation in the NF1 gene in a Brazilian patient with ectropion uveae
(Karger, 2004-01-01)
Congenital ectropion uveae is a rare, nonprogressive anomaly characterized by the presence of iris pigment epithelium on the anterior surface of the iris stroma and is occasionally associated with Rieger's anomaly, ...