Contiguous gene syndrome due to an interstitial deletion in Xp22.3 in a boy with ichthyosis, chondrodysplasia punctata, mental retardation and ADHD.
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| Description | scientific article published on 21 May 2007 |
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author: Orsetta Zuffardi Manuela De Gregori Fortunato Lonardo Gioacchino Scarano Nicola Brunetti-Pierri |
| Publication date | May 21, 2007 |
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