A novel syndrome of congenital lid and punctal anomalies, corneal and chorioretinal dystrophy

Ophthalmic Genetics

Volumn 24, Issue 2, 2003, Pages 111-116

  Lee, Thomas K M ^a   Hébert, Marc ^b   MacDonald, Ian M ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

^b NONE

Author keywords

Chorioretinal dystrophy; Corneal dystrophy; Lacrimal punctum

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CONGENITAL CORNEA DYSTROPHY; ELECTRORETINOGRAPHY; EPIPHORA; EYE DISEASE; EYELID DISEASE; FEMALE; GENE MUTATION; HUMAN; LACRIMAL APPARATUS; PHOTOPHOBIA; PRIORITY JOURNAL; RETINA MACULA DEGENERATION;

ADULT; CORNEAL DYSTROPHIES, HEREDITARY; DNA-BINDING PROTEINS; EYE ABNORMALITIES; EYE PROTEINS; EYELIDS; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; HOMEODOMAIN PROTEINS; HUMANS; LACRIMAL APPARATUS; PAIRED BOX TRANSCRIPTION FACTORS; REPRESSOR PROTEINS; RETINAL DEGENERATION; SYNDROME; TRANSCRIPTION FACTORS;

EPIPHORA; POMACANTHUS MACULOSUS;

EID: 0038331658     PISSN: 13816810     EISSN: None     Source Type: Journal    
DOI: 10.1076/opge.24.2.111.13995     Document Type: Article

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