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Volumn 59, Issue 7, 2002, Pages 1147-1153

Interrelationship of genetics and prenatal injury in the genesis of malformations of cortical development

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGYRIA; ARTICLE; BRAIN MALFORMATION; BRAZIL; CHILD; CONTROLLED STUDY; CORTICAL DYSPLASIA; DIAGNOSTIC IMAGING; DISEASE ASSOCIATION; ENVIRONMENTAL FACTOR; EPILEPSY; FAMILY HISTORY; FEMALE; FETUS DISEASE; GENETIC ASSOCIATION; GENETIC RISK; HEREDITY; HETEROTOPIA; HUMAN; IMAGE ANALYSIS; INJURY; MAJOR CLINICAL STUDY; MALE; MICROGYRIA; MORPHOGENESIS; NEUROLOGIC DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PACHYGYRIA; PRIORITY JOURNAL; RISK ASSESSMENT; RISK FACTOR; SCHIZENCEPHALY;

EID: 0036311166     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.59.7.1147     Document Type: Article
Times cited : (64)

References (34)
  • 8
    • 0032498306 scopus 로고    scopus 로고
    • Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome; encodes a putative signaling protein
    • (1998) Cell , vol.92 , pp. 63-72
    • Gleeson, J.G.1    Allen, K.M.2    Fox, J.W.3
  • 10
    • 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.