Axenfeld-Rieger syndrome: New perspectives

British Journal of Ophthalmology

Volumn 96, Issue 3, 2012, Pages 318-322

  Chang, Ta C ^a   Summers, C Gail ^b   Schimmenti, Lisa A ^b   Grajewski, Alana L ^b,c  

^a VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^b UNIVERSITY OF MINNESOTA   (United States)

^c UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

Author keywords

Anterior segment dysgenesis; Axenfeld; Rieger

Indexed keywords

ANTERIOR EYE SEGMENT; AXENFELD RIEGER SYNDROME; CARDIOVASCULAR MALFORMATION; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE SEVERITY; ENDOCRINE DISEASE; FOXC1 GENE; GENE MUTATION; GENE PRODUCT; GENETIC DISORDER; GLAUCOMA; HEART DISEASE; HEART OUTFLOW TRACT OBSTRUCTION; HUMAN; HYPOPHYSIS DISEASE; MOLECULAR DIAGNOSIS; MOLECULAR GENETICS; OUTCOME ASSESSMENT; PERCEPTION DEAFNESS; PITX2 GENE; PRIORITY JOURNAL; REVIEW; RISK FACTOR; TRABECULOTOMY;

ANTERIOR EYE SEGMENT; EYE ABNORMALITIES; FORKHEAD TRANSCRIPTION FACTORS; HOMEODOMAIN PROTEINS; HUMANS; TRANSCRIPTION FACTORS;

EID: 84857118708     PISSN: 00071161     EISSN: 14682079     Source Type: Journal    
DOI: 10.1136/bjophthalmol-2011-300801     Document Type: Review

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