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Volumn 37, Issue 4, 2005, Pages 237-244

Comprehensive developmental glaucoma classification

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOOSTEOHYPERTROPHY SYNDROME; ANIRIDIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AXENFELD RIEGER SYNDROME; BASAL CELL NEVUS SYNDROME; BING NEEL SYNDROME; BLACKFAN DIAMOND ANEMIA; CATARACT; CATARACT EXTRACTION; CHROMOSOME 11Q; CHROMOSOME DELETION; CLINICAL FEATURE; COCKAYNE SYNDROME; CONGENITAL ECTROPION UVEA; CONGENITAL HYPOTHYROIDISM; CONGENITAL IRIS HYPOPLASIA; CONGENITAL RUBELLA SYNDROME; CORNEA DISEASE; CYSTINOSIS; CYTOMEGALIC INCLUSION BODY DISEASE; DENTAL OCULAR CUTANEOUS SYNDROME; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; EDWARDS SYNDROME; EYE MALFORMATION; FAMILIAL HISTIOCYTIC DERMATOARTHRITIS; FETAL ALCOHOL SYNDROME; GLAUCOMA; HALLERMANN STREIFF SYNDROME; HOMOCYSTINURIA; HUMAN; HURLER SYNDROME; INFECTION; IRIS DISEASE; JUVENILE XANTHOGRANULOMA; KARTAGENER SYNDROME; KIDNEY DISEASE; KRAUSE SYNDROME; LOWE SYNDROME; MANDIBULOFACIAL DYSOSTOSIS; MARFAN SYNDROME; MEGALOCORNEA; METABOLIC DISORDER; MICROCORNEA; MILLER FINEMAN SMITH SYNDROME; MUSCULOSKELETAL DISEASE; NEUROEPITHELIOMA; NEUROFIBROMATOSIS; NEUROLOGIC DISEASE; OCULODENTODIGITAL SYNDROME; PARTIAL TRISOMY 9; PATAU SYNDROME; PEDIATRIC SURGERY; PERICENTRIC CHROMOSOME INVERSION; PETERS ANOMALY; PIERRE ROBIN SYNDROME; POSTOPERATIVE COMPLICATION; PRADER WILLI SYNDROME; RETINOBLASTOMA; RETINOSCHISIS; RETROLENTAL FIBROPLASIA; RUBINSTEIN SYNDROME; SHAKEN BABY SYNDROME; STICKLER SYNDROME; TELANGIECTASIA; TRISOMY 21; TURNER SYNDROME; VON HIPPEL LINDAU DISEASE; WAARDENBURG SYNDROME; WEILL MARCHESANI SYNDROME; X LINKED MENTAL RETARDATION; ZELLWEGER SYNDROME;

EID: 31644441259     PISSN: 15304086     EISSN: None     Source Type: Journal    
DOI: 10.1385/AO:37:4:237     Document Type: Article
Times cited : (5)

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