Polymicrogyria: A common and heterogeneous malformation of cortical development

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

Volumn 166, Issue 2, 2014, Pages 227-239

  Stutterd, Chloe A ^a   Leventer, Richard J ^b  

^a MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

^b ROYAL CHILDREN'S HOSPITAL   (Australia)

Author keywords

Malformation of cortical development; Polymicrogyria; Schizencephaly

Indexed keywords

ALPHA TUBULIN; BETA TUBULIN; GLUTAMATE RECEPTOR; PHOSPHATIDYLINOSITOL 3 KINASE;

ADRENOLEUKODYSTROPHY; AGYRIA; ALEXANDER DISEASE; ANEUPLOIDY; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAIN CORTEX; BRAIN MALFORMATION; BRAIN VENTRICLE; CEREBELLUM CORTEX; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CLINICAL FEATURE; COBBLESTONE LISSENCEPHALY; COMPUTER ASSISTED TOMOGRAPHY; CORPUS CALLOSUM AGENESIS; CORTICAL DYSPLASIA; CYTOMEGALOVIRUS INFECTION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; FACIAL NERVE PARALYSIS; GENE DELETION; GENE MUTATION; GENETIC COUNSELING; GRAY MATTER; HETEROTOPIA; HIPPOCAMPUS; HUMAN; INTELLECTUAL IMPAIRMENT; MACROGYRIA; MICROGYRIA; MOTOR DYSFUNCTION; MYELINATION; NEUROIMAGING; NEUROLOGIST; NEURONAL MIGRATION DISORDER; NOMENCLATURE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PRENATAL CARE; PRIORITY JOURNAL; PROTEIN DOMAIN; RECESSIVE GENE; SIGNAL NOISE RATIO; SUBARACHNOID SPACE; ZELLWEGER SYNDROME; ANIMAL; GENETIC HETEROGENEITY; GENETICS; MUTATION; PATHOLOGY;

ANIMALS; CEREBRAL CORTEX; CHROMOSOME ABERRATIONS; GENETIC HETEROGENEITY; HUMANS; MAGNETIC RESONANCE IMAGING; MUTATION; NEUROIMAGING; POLYMICROGYRIA;

EID: 84902535810     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.31399     Document Type: Article

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