| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5907251 | Gene | 2012 | 4 Pages |
Abstract
⺠A case of neonatal diagnosis of 49,XXXXY syndrome is presented. ⺠Identification was prompted by a bilateral thickening of the radioulnar joints. ⺠In contrast to previous reports, radioulnar synostosis was present at birth. ⺠Microsatellite analysis showed two diverse X chromosomes, each present in two copies.
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Authors
André Kidszun, Anne-Jule Fuchs, Alexandra Russo, Marius Bartsch, Gabriele Frey-Mahn, Vera Beyer, Ulrich Zechner, Oliver Bartsch, Eva Mildenberger,