A child with sclerocornea, short limbs, short stature, and distinct facial appearance
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference8 articles.
1. Classification of Corneal Endothelial Disorders Based on Neural Crest Origin
2. Mesenchymal dysgenesis in Peters' anomaly, sclerocornea and congenital endothelial dystrophy
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1. Hydrocephalus, agenesis of the corpus callosum, and cleft lip/palate represent frequent associations in fetuses with Peters' plus syndrome and B3GALTL mutations. - Fetal PPS phenotypes, expanded by Dandy Walker cyst and encephalocele;Prenatal Diagnosis;2012-11-13
2. Pediatric Keratoplasty;Survey of Ophthalmology;2009-03
3. Apple peel intestinal atresia in siblings with ocular anomalies and microcephaly;Clinical Genetics;2008-04-23
4. A Review of Anterior Segment Dysgeneses;Survey of Ophthalmology;2006-05
5. Congenital Hypothyroidism in Peters Plus Syndrome;Ophthalmic Genetics;2006-01
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