6 results on '"Schilter K"'
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2. OTX2 microphthalmia syndrome: four novel mutations and delineation of a phenotype
3. 483 Rare constitutional variants influence phenotype of somatic cutaneous vascular malformations
4. Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies
5. Diffuse Leptomeningeal Histiocytic Sarcoma: Histologic and Molecular Findings in an Autopsy Case.
6. Variability of Delivery of Timolol for the Treatment of Infantile Hemangiomas.
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