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- W2004163760 abstract "Chromosome 13q deletion syndrome is characterized by growth retardation, cognitive delays, and organ and musculoskeletal deformities. Typical ocular associations include retinoblastoma, microphthalmia, and colobomas. We report a case of bilateral iris heterochromia and retinal pigment abnormalities in a child with 13q-syndrome." @default.
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- W2004163760 date "2007-10-01" @default.
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- W2004163760 title "Sectoral iris heterochromia and retinal pigment variation in 13q-syndrome" @default.
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- W2004163760 doi "https://doi.org/10.1016/j.jaapos.2007.04.012" @default.
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