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Volumn 19, Issue 4, 2005, Pages 396-399

The prevalence and associated features of posterior embryotoxon in the general ophthalmic clinic

Author keywords

Alagille's syndrome; Anterior segment dysgenesis; Axenfeld Reiger syndrome; Posterior embryotoxon

Indexed keywords

ADOLESCENT; ADULT; AGE DISTRIBUTION; AGED; ANIRIDIA; ANTERIOR EYE SEGMENT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AXENFELD REIGER SYNDROME; CHILD; CLINICAL FEATURE; CORNEA DISEASE; GENETIC DISORDER; GLAUCOMA; GONIOSCOPY; HUMAN; INTRAOCULAR HYPERTENSION; KERATOMETRY; MAJOR CLINICAL STUDY; PIGMENTATION; POSTERIOR EMBRYOTOXON; PREVALENCE; RISK ASSESSMENT; SLIT LAMP; SYSTEMIC DISEASE;

EID: 17544364757     PISSN: 0950222X     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.eye.6701508     Document Type: Article
Times cited : (43)

References (12)
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  • 3
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  • 9
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    • Axenfeld-Rieger syndrome: A theory of mechanism and distinctions from the iridocorneal endothelial syndrome
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    • Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peter's anomaly
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    • JAGGED1 expression in human embryos: Correlation with the Alagille syndrome phenotype
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.