WAGR syndrome and multiple exostoses in a patient with del (11) (p11.2p14.2)

J. M. McGaughran, H. B. Ward, D. G R Evans

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The WAGR syndrome (Wilms' tumour, aniridia, genital anomalies, and mental retardation) is well documented to be associated with a deletion of 11pl3. We present a patient with a del(11)(pll.2p14.2) who as well as all the features of WAGR syndrome has multiple exostoses. We suggest that this could be a possible locus for hereditary multiple exostoses.
    Original languageEnglish
    Pages (from-to)823-824
    Number of pages1
    JournalJournal of Medical Genetics
    Volume32
    Issue number10
    DOIs
    Publication statusPublished - 1995

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