Benign idiopathic partial seizures in the velocardiofacial syndrome: Report of two cases

This publication has 11 references indexed in Scilit:

• Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice
  Nature, 2001
• DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
  Nature Genetics, 2001
• TBX1 Is Responsible for Cardiovascular Defects in Velo-Cardio-Facial/DiGeorge Syndrome
  Published by Elsevier ,2001
• Cortical dysgenesis in 2 patients with chromosome 22q11 deletion
  Clinical Genetics, 2000
• Velo-cardio-facial syndrome: A distinctive behavioral phenotype
  Mental Retardation and Developmental Disabilities Research Reviews, 2000
• Centrotemporal spikes in families with rolandic epilepsy
  Neurology, 1998
• Benign Childhood Epilepsy with Centrotemporal Spikes and Electroencephalography Trait are Not Linked to EBN1 and EBN2 of Benign Neonatal Familial Convulsions
  Epilepsia, 1997
• Benign Childhood Epilepsy with Centrotemporal Spikes and the Focal Sharp Wave Trait is not Linked to the Fragile X Region
  Neuropediatrics, 1993
• Benign childhood epilepsy with occipital paroxysms: A 15‐year prospective study
  Annals of Neurology, 1989
• The velo-cardio-facial (Shprintzen) syndrome
  European Journal of Pediatrics, 1986