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A novel Xp22.11 deletion causing a syndrome of craniosynostosis and periventricular nodular heterotopia

Margriet van Kogelenberg1, Margherita Lerone, Teresa De Toni

  • 1Department of Paediatrics and Child Health, Dunedin School of Medicine, Otago University, Dunedin, New Zealand.

American Journal of Medical Genetics. Part A
|November 5, 2011
PubMed

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