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3. Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders

8. Refractive errors in patients with Bardet Biedl syndrome.

11. The Surviving, Not Thriving, Photoreceptors in Patients with ABCA4 Stargardt Disease.

12. Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD

27. Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing

29. TUBB4Bvariants specifically impact ciliary function, causing a ciliopathic spectrum

33. List of Contributors

35. Modelling eye lengths and refractions in the periphery.

37. The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences

38. The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences

41. The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences

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