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Publications by Jan Willem R. Pott
Novel Membrane Frizzled-Related Protein Gene Mutation as Cause of Posterior Microphthalmia Resulting in High Hyperopia With Macular Folds
Acta Ophthalmologica
Medicine
Ophthalmology
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Macular Degeneration Associated With a Novel Treacher Collins Tcof1 Mutation and Evaluation of This Mutation in Age Related Macular Degeneration
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Molecular Neuroscience
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Novel Truncation Mutations in MYRF Cause Autosomal Dominant High Hyperopia Mapped to 11p12–q13.3
Human Genetics
Genetics
Unique Presentation of Congenital Cataract Concurrent With Microcornea, Microphthalmia Plus Posterior Capsule Defect in Monozygotic Twins Caused by a Novel GJA8 Mutation
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
Novel Mutations in PXDN Cause Microphthalmia and Anterior Segment Dysgenesis
European Journal of Human Genetics
Genetics
Structural Characteristics of Novel Protein Folds
PLoS Computational Biology
Molecular Neuroscience
Evolution
Ecology
Genetics
Behavior
Molecular Biology
Systematics
Simulation
Cellular
Computational Theory
Mathematics
Modeling
A Patient With Posterior Cortical Atrophy Possesses a Novel Mutation in the Presenilin 1 Gene
PLoS ONE
Multidisciplinary
A Novel Monoclonal Antibody to Secreted Frizzled-Related Protein 2 Inhibits Tumor Growth
Molecular Cancer Therapeutics
Cancer Research
Oncology
Secreted Frizzled-Related Protein-1 (sFRP-1)
Science-Business eXchange
Novel Prion Protein Gene Mutation in an Octogenarian With Creutzfeldt-Jakob Disease
Archives of Neurology
