Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia

Ophthalmology

Volumn 108, Issue 7, 2001, Pages 1313-1322

  Flaherty, Maree P ^a   Grattan Smith, Padraic ^a   Steinberg, Adam ^a   Jamieson, Robyn ^a   Engle, Elizabeth C ^b  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BASAL GANGLION; BRAIN DEVELOPMENT; CASE REPORT; CAUDATE NUCLEUS; CHILD; CHROMOSOME 12; CHROMOSOME DELETION; CLINICAL FEATURE; CORTICAL DYSPLASIA; DISEASE ASSOCIATION; EXTRAOCULAR MUSCLE; FEMALE; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; MYOFIBROSIS; PRIORITY JOURNAL; PUTAMEN;

ABNORMALITIES, MULTIPLE; ADULT; BASAL GANGLIA; BLEPHAROPTOSIS; CEREBRAL CORTEX; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 12; EYE ABNORMALITIES; EYE MOVEMENTS; FEMALE; FIBROSIS; HUMANS; LINKAGE (GENETICS); LOD SCORE; MAGNETIC RESONANCE IMAGING; OCULOMOTOR MUSCLES; OPHTHALMOPLEGIA; PEDIGREE;

EID: 0034971195     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(01)00582-6     Document Type: Article

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