DOI: 10.1055/s-00029025

Journal of Pediatric Epilepsy

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References

Béna F, Bottani A, Marcelli F, Sizonenko LD, Conrad B, Dahoun S.
A de novo 1.1-1.6 Mb subtelomeric deletion of chromosome 20q13.33 in a patient with learning difficulties but without obvious dysmorphic features.

Am J Med Genet A 2007;
143A (16) 1894-1899

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