Peters Anomaly
Peters Anomaly is a congenital ocular disorder characterized by central corneal opacity due to defects in the posterior corneal stroma, Descemet’s membrane, and endothelium, often associated with iridocorneal or lenticulocorneal adhesions, and representing a distinct subtype of anterior segment dysgenesis.
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A mutation in the RIEG1 gene associated with Peters’ anomaly
W Doward, Rahat Perveen, I. Christopher Lloyd et al. · Journal of Medical Genetics · 1999 · 155 citations · Full text
<i>PAX6</i> Mutation as a Genetic Factor Common to Aniridia and Glucose Intolerance
Tetsuyuki Yasuda, Yoshitaka Kajimoto, Yoshio Fujitani et al. · Diabetes · 2002 · 143 citations · Full text
Child-Centred Education and Its Critics
O. R. Omole, John R. Darling · British Journal of Educational Studies · 1995 · 120 citations
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Johns Hopkins University
Baltimore, United States
6 h-index
14 publications
481 citations

Medical College of Wisconsin
Milwaukee, United States
6 h-index
20 publications
980 citations
University of Illinois Chicago
Chicago, United States
5 h-index
10 publications
230 citations

Wills Eye Hospital
Philadelphia, United States
5 h-index
14 publications
843 citations

Westchester Medical Center
Valhalla, United States
4 h-index
12 publications
553 citations
Children's Hospital of Wisconsin
Milwaukee, United States
4 h-index
12 publications
536 citations

Tel Aviv University
Tel Aviv, Israel
4 h-index
6 publications
154 citations
Johns Hopkins Hospital
Baltimore, United States
3 h-index
12 publications
634 citations
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11 publications · 644 citations
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11 publications · 364 citations
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9 publications · 203 citations
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Repository · 7 publications · 259 citations
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6 publications · 188 citations
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