Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations

Investigative Ophthalmology and Visual Science

Volumn 48, Issue 1, 2007, Pages 228-237

  Strungaru, M Hermina ^a   Dinu, Irina ^a   Walter, Michael A ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL FEATURE; FEMALE; FOXC1 GENE; GENE; GENE MUTATION; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; GLAUCOMA; HUMAN; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PHENOTYPE; PITX2 GENE; PRIORITY JOURNAL; PROGNOSIS; RIEGER SYNDROME; SEX RATIO; ANTERIOR EYE SEGMENT; CONGENITAL MALFORMATION; EYE MALFORMATION; FILTERING OPERATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; INTRAOCULAR PRESSURE; IRIS; MUTATION; POLYMERASE CHAIN REACTION; RETROSPECTIVE STUDY;

ANTIHYPERTENSIVE AGENT; FORKHEAD TRANSCRIPTION FACTOR; FOXC1 PROTEIN, HUMAN; HOMEODOMAIN PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR PITX2; UNCLASSIFIED DRUG;

ANTERIOR EYE SEGMENT; ANTIHYPERTENSIVE AGENTS; EYE ABNORMALITIES; FEMALE; FILTERING SURGERY; FORKHEAD TRANSCRIPTION FACTORS; GENOTYPE; GLAUCOMA; HOMEODOMAIN PROTEINS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTRAOCULAR PRESSURE; IRIS; MALE; MUTATION; PHENOTYPE; POLYMERASE CHAIN REACTION; PROGNOSIS; RETROSPECTIVE STUDIES; TRANSCRIPTION FACTORS;

EID: 33846907614     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: 10.1167/iovs.06-0472     Document Type: Article

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