Electroclinical features of epilepsy associated with 1p36 deletion syndrome: A review
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference54 articles.
1. Monosomy 1p36–A multifaceted and still enigmatic syndrome: four clinically diverse cases with shared white matter abnormalities;Õiglane-Shlik;Eur. J. Paediatr. Neurol.,2014
2. Spectrum of epilepsy in terminal 1p36 deletion syndrome;Bahi-Buisson;Epilepsia,2008
3. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia;Pediatrics,2008
4. Del 1p36 syndrome: a newly emerging clinical entity;Battaglia;Brain Dev.,2005
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