| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3053904 | European Journal of Paediatric Neurology | 2012 | 6 Pages |
Abstract
Background and objectivesPallister–Killian syndrome (PKS) is a rare genetic disorder caused by a tissue-limited mosaic supernumerary isochromosome 12p. Typical facial dysmorphisms, pigmentary abnormalities, and some major malformations are frequently present. Neurologica
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Authors
Lucio Giordano, Maurizio Viri, Renato Borgatti, Monica Lodi, Patrizia Accorsi, Francesca Faravelli, Maria Chiara Ferretti, Rita Grasso, Luigi Memo, Silvia Prola, Dario Pruna, Margherita Santucci, Salvatore Savasta, Alberto Verrotti, Antonino Romeo,