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Volumn 51, Issue 3, 2002, Pages 340-349

X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): Clinical, magnetic resonance imaging, and neuropathological findings

Author keywords

[No Author keywords available]

Indexed keywords

AGYRIA; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; CORPUS CALLOSUM; GENITAL MALFORMATION; HISTOPATHOLOGY; HUMAN; MULTIGENE FAMILY; NEUROLOGIC DISEASE; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; PACHYGYRIA; PRIORITY JOURNAL; WHITE MATTER; X CHROMOSOME LINKAGE;

EID: 0036199532     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10119     Document Type: Article
Times cited : (134)

References (12)
  • 5
    • 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
  • 6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.