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Volumn 59, Issue 9, 2002, Pages 1476-1479

Mesial temporal lobe abnormalities in a family with 15q26qter trisomy

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BEHAVIOR DISORDER; BRAIN CORTEX LESION; CASE REPORT; CHROMOSOME 15Q; CHROMOSOME TRANSLOCATION 12; CHROMOSOME TRANSLOCATION 15; ELECTROENCEPHALOGRAM; FACE DYSMORPHIA; FAMILIAL DISEASE; GENERALIZED EPILEPSY; GENETIC ASSOCIATION; HIPPOCAMPUS; HUMAN; KARYOTYPING; MALE; MENTAL DEFICIENCY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SIBLING; SUBICULUM; TEMPORAL LOBE; TRISOMY; TRISOMY 15Q;

EID: 0036719023     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.59.9.1476     Document Type: Article
Times cited : (11)

References (11)
  • 11
    • 17444444915 scopus 로고    scopus 로고
    • A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
    • (1998) Cell , vol.92 , pp. 51-61
    • Des Portes, V.1    Pinard, J.M.2    Billuart, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.