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Publications by J C Sowden

Molecular and Developmental Mechanisms of Anterior Segment Dysgenesis

Sensory Systems

English

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Novel Mutations in PXDN Cause Microphthalmia and Anterior Segment Dysgenesis

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Foxf2: A Novel Locus for Anterior Segment Dysgenesis Adjacent to the Foxc1 Gene

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TASP1 Mutation in a Female With Craniofacial Anomalies, Anterior Segment Dysgenesis, Congenital Immunodeficiency and Macrocytic Anemia

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Molecular Mechanisms of Midfacial Developmental Defects

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Mutation Analysis of the Genes Associated With Anterior Segment Dysgenesis, Microcornea and Microphthalmia in 257 Patients With Glaucoma

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Classification of Ocular Anterior Dysgenesis: New Insights

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Deletion of G Protein-Coupled Receptor 48 Leads to Ocular Anterior Segment Dysgenesis (ASD) Through Down-Regulation of Pitx2

Proceedings of the National Academy of Sciences of the United States of America

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What's New in Ocular Anterior Dysgenesis Imaging?

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High Resolution Anterior Segment OCT CASIA 2 for Corneal and Anterior Segment Diagnosis

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