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Showing results 11 to 15 of 15

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Issue Date	Title	Journal Title
2021	Serial Detection of MYD88 L265P Mutation in the Aqueous Humor of a Patient with Vitreoretinal Lymphoma for Disease Monitoring	OCULAR IMMUNOLOGY AND INFLAMMATION
2020	SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization	HUMAN MOLECULAR GENETICS
2019	Targeted panel sequencing identifies a novel NR2F1 mutations in a patient with Bosch-Boonstra-Schaaf optic atrophy syndrome	Ophthalmic Genetics
2021	TUBB3 M323V Syndrome Presents with Infantile Nystagmus	GENES
2020	Whole exome sequencing identifies mutational signatures of vitreoretinal lymphoma	HAEMATOLOGICA