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Sclerocornea

A congenital anomaly in which a part or the whole of the cornea acquires the characteristics of sclera, resulting in clouding of the cornea. [HPO… Expand
National Institutes of Health

Papers overview

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Highly Cited
2016
Highly Cited
2016
ABSTRACT Congenital cataracts are a significant cause of lifelong visual loss. They may be isolated or associated with… Expand
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Highly Cited
2011
Highly Cited
2011
BMP4 loss-of-function mutations and deletions have been shown to be associated with ocular, digital, and brain anomalies, but due… Expand
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Highly Cited
2009
Highly Cited
2009
FOXE3 is a lens-specific transcription factor with a highly conserved forkhead domain previously implicated in congenital primary… Expand
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Highly Cited
2007
Highly Cited
2007
OBJECTIVE To examine characteristics of circumcised and uncircumcised Latino and black men who have sex with men (MSM) in the… Expand
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Highly Cited
2005
Highly Cited
2005
Heterozygous, de novo, loss-of-function mutations in SOX2 have been shown to cause bilateral anophthalmia. Here we provide a… Expand
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Highly Cited
2004
Highly Cited
2004
Anophthalmia and microphthalmia are among the most common ocular birth defects and a significant cause of congenital blindness… Expand
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Highly Cited
1994
Highly Cited
1994
Limbal allograft transplantation was performed consecutively in 16 eyes with thermal or chemical burns (n = 5), Terrien's… Expand
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Review
1993
Review
1993
Bilateral microphthalmia with blepharophimosis, linear lesions of dermal aplasia involving the face, and microcephaly were… Expand
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1985
1985
Sclerocornea is a primary anomaly in which scleralization of a peripheral part of the cornea, or the entire corneal tissue… Expand
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Review
1975
Review
1975
Abstract Among the congenital malformations of the ocular anterior segment, Peters' anomaly, sclerocornea and cogenital… Expand
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