SCOPUS 정보 검색 플랫폼

Neurology

Volumn 57, Issue 6, 2001, Pages 1108-1111

Ring chromosome 20 epilepsy syndrome in children: Electroclinical features

(6) Augustijn, P B a,d Parra, J a Wouters, C H b Joosten, P b Lindhout, D c Van Emde Boas, W a

a STICHTING EPILEPSIE INSTELLINGEN NEDERLAND SEIN (Netherlands)

b ERASMUS MEDICAL CENTER (Netherlands)

c UNIVERSITY MEDICAL CENTER UTRECHT (Netherlands)

d Meer en Bosch and De Cruquiushoeve (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; BENIGN CHILDHOOD EPILEPSY; CASE REPORT; CHROMOSOME 20; CHROMOSOME MOSAICISM; CLINICAL FEATURE; COGNITIVE DEFECT; ELECTROENCEPHALOGRAM; EPILEPTIC STATE; FACE DYSMORPHIA; FEMALE; FRONTAL LOBE EPILEPSY; GENETIC ASSOCIATION; HUMAN; INTRACTABLE EPILEPSY; MALE; MENTAL DEFICIENCY; PRIORITY JOURNAL; RING CHROMOSOME; SCHOOL CHILD;

EID: 0035949744 PISSN: 00283878 EISSN: None Source Type: Journal
DOI: 10.1212/WNL.57.6.1108 Document Type: Article

Times cited : (55)

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