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- W2017294839 abstract "Peters9 anomaly is usually a sporadic or autosomal recessive condition. We present three families whose members had dominantly inherited anterior segment anomalies with variable expression, including typical Peters9 anomaly in at least one family member. Slit-lamp examination of parents and family members of children with Peters9 anomaly is therefore important to exclude dominant inheritance." @default.
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- W2017294839 date "1991-10-01" @default.
- W2017294839 modified "2023-09-28" @default.
- W2017294839 title "Heterogeneity in dominant anterior segment malformations." @default.
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- W2017294839 doi "https://doi.org/10.1136/bjo.75.10.591" @default.
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