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 language | English |
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Pages (from-to) | 823-824 |
Number of pages | 1 |
Journal | Journal of Medical Genetics |
Volume | 32 |
Issue number | 10 |
DOIs | |
Publication status | Published - 1995 |