The genetics of lissencephaly

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

Volumn 166, Issue 2, 2014, Pages 198-210

  Fry, Andrew E ^a   Cushion, Thomas D ^b   Pilz, Daniela T ^c  

^a UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

^b SWANSEA UNIVERSITY   (United Kingdom)

^c NONE

Author keywords

Agyria; DCX; Genetics; LIS1; Lissencephaly; Pachygyria; PAFAH1B1; Subcortical band heterotopia; TUBA1A

Indexed keywords

ALPHA DYSTROGLYCAN; HOMEODOMAIN PROTEIN;

AGYRIA; ARTICLE; BARAITSER WINTER SYNDROME; BASAL GANGLION; BRAIN STEM; CEREBELLUM HYPOPLASIA; CEREBROFRONTOFACIAL SYNDROME TYPE 3; COBBLESTONE LISSENCEPHALY; CORPUS CALLOSUM; FRYNS AFTIMOS SYNDROME; GENE MUTATION; GENETICS; GENITAL SYSTEM; GLYCOSYLATION; HEAD CIRCUMFERENCE; HIPPOCAMPUS; HISTOPATHOLOGY; HUMAN; MALFORMATION SYNDROME; MICROCEPHALY; MICROLISSENCEPHALY; MISSENSE MUTATION; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; RARE DISEASE; ANIMAL; GENETIC HETEROGENEITY; MUTATION; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOLOGY;

ANIMALS; GENETIC HETEROGENEITY; HUMANS; LISSENCEPHALY; MAGNETIC RESONANCE IMAGING; MUTATION; NEUROIMAGING; PHENOTYPE;

EID: 84902440733     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.31402     Document Type: Article

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