The clinical patterns and molecular genetics of lissencephaly and subcortical band heterotopia: Malformations of cortical development - Genetics

Epilepsia

Volumn 51, Issue SUPPL. 1, 2010, Pages 5-9

  Dobyns, William B ^a  

^a UNIVERSITY OF CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AGYRIA; BRAIN CORTEX; BRAIN MALFORMATION; CLINICAL FEATURE; CONFERENCE PAPER; GENE MUTATION; HUMAN; MOLECULAR GENETICS; NEUROIMAGING; PRIORITY JOURNAL; SUBCORTICAL HETEROTOPIA;

CEREBELLUM; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; CLASSICAL LISSENCEPHALIES AND SUBCORTICAL BAND HETEROTOPIAS; CORPUS CALLOSUM; FEMALE; GASTROESOPHAGEAL REFLUX; GENE EXPRESSION; HUMANS; LISSENCEPHALY; MALE; POINT MUTATION;

EID: 76249099322     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2009.02433.x     Document Type: Conference Paper

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