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American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 97, Issue 3, 2000, Pages 213-220

X-linked malformations of cortical development

(3) Leventer, Richard J a Mills, Patti L b Dobyns, William B a

a UNIVERSITY OF CHICAGO (United States)

b University of Chicago ^*

Author keywords

Band heterotopia; Cortical malformation; Doublecortin; Filamin 1; Lissencephaly; Nodular heterotopia; Polymicrogyria

Indexed keywords

DOUBLECORTIN; FILAMIN;

AGYRIA; ARTICLE; BRAIN CORTEX; BRAIN DEVELOPMENT; BRAIN MALFORMATION; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; DISEASE CLASSIFICATION; EPILEPSY; GENETIC PREDISPOSITION; HETEROTOPIA; HUMAN; MALFORMATION SYNDROME; MENTAL DEFICIENCY; MICROGYRIA; NEUROLOGIC DISEASE; PRIORITY JOURNAL; SUPRASYLVIAN GYRUS; X CHROMOSOMAL INHERITANCE; X CHROMOSOME LINKED DISORDER;

BRAIN DISEASES; CEREBRAL CORTEX; GENETIC COUNSELING; HUMANS; LINKAGE (GENETICS); UROGENITAL ABNORMALITIES; X CHROMOSOME;

GENETTA;

EID: 0034521813 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/1096-8628(200023)97:3<213::AID-AJMG1039>3.0.CO;2-W Document Type: Article

Times cited : (19)

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