A developmental and genetic classification for malformations of cortical development

Neurology

Volumn 65, Issue 12, 2005, Pages 1873-1887

  Barkovich, A J ^a,f   Kuzniecky, R I ^b   Jackson, G D ^c   Guerrini, R ^d   Dobyns, W B ^e  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b NEW YORK UNIVERSITY MEDICAL CENTER   (United States)

^c UNIVERSITY OF MELBOURNE   (Australia)

^d DEPARTMENT OF DEVELOPMENTAL NEUROSCIENCE   (Italy)

^e UNIVERSITY OF CHICAGO   (United States)

^f NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID; FUKUTIN;

APOPTOSIS; BRAIN BIOPSY; BRAIN DEVELOPMENT; BRAIN MALFORMATION; CELL MIGRATION; CELL PROLIFERATION; CHROMOSOME MOSAICISM; DEVELOPMENTAL DISORDER; DISEASE CLASSIFICATION; EMBRYO DEVELOPMENT; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE; HETEROTOPIA; HOMOZYGOSITY; HUMAN; MICROCEPHALY; NERVE CELL; NEUROIMAGING; NEUROPATHOLOGY; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; REVIEW; SYNDROME DELINEATION; X CHROMOSOME INACTIVATION; BRAIN CORTEX; CLASSIFICATION; CONGENITAL MALFORMATION; DIAGNOSTIC IMAGING; DIFFERENTIAL DIAGNOSIS; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETICS; MUTATION; NERVOUS SYSTEM MALFORMATION; NUCLEOTIDE SEQUENCE; STANDARD;

CEREBRAL CORTEX; DIAGNOSIS, DIFFERENTIAL; DIAGNOSTIC IMAGING; DNA MUTATIONAL ANALYSIS; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HUMANS; MUTATION; NERVOUS SYSTEM MALFORMATIONS;

EID: 32144433872     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000183747.05269.2d     Document Type: Review

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