A novel hereditary developmental vitreoretinopathy with multiple ocular abnormalities ocalizing to a f-cM region of chromosome fq13-q14

GCM Black, R Perveen, W Wiszniewski, CL Dodd, D Donnai, D McLeod

    Research output: Contribution to journalArticlepeer-review

    Original languageEnglish
    JournalOphthalmology
    Volume106
    Publication statusPublished - 1999

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