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  1. 2017

  2. LONG-TERM FOLLOW-UP OF PATIENTS WITH RETINITIS PIGMENTOSA TYPE 12 CAUSED BY CRB1 MUTATIONS: A Severe Phenotype With Considerable Interindividual Variability

    Mathijssen, I. B., Florijn, R. J., van den Born, L. I., Zekveld-Vroon, R. C., ten Brink, J. B., Plomp, A. S., Baas, F., Meijers-Heijboer, H., Bergen, A. A. B. & van Schooneveld, M. J., 2017, In: Retina (Philadelphia, Pa.). 37, 1, p. 161-172

    Research output: Contribution to journal › Article › Academic › peer-review

  3. 2012

  4. Clinical Course, Genetic Etiology, and Visual Outcome in Cone and Cone-Rod Dystrophy

    Thiadens, A. A. H. J., Phan, T. M. L., Zekveld-Vroon, R. C., Leroy, B. P., van den Born, L. I., Hoyng, C. B., Klaver, C. C. W., Roosing, S., Pott, J-W. R., Schooneveld, M. J. V., Moll-Ramirez, N. V., Genderen, M. M. V., Boon, C. J. F., Hollander, A. I. D., Bergen, A. A. B., Baere, E. D., Cremers, F. P. M. & Lotery, A. J., 2012, In: Ophthalmology. 119, 4, p. 819-826

    Research output: Contribution to journal › Article › Academic › peer-review

  5. 2009

  6. Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders

    Thiadens, A. A. H. J., den Hollander, A. I., Roosing, S., Nabuurs, S. B., Zekveld-Vroon, R. C., Collin, R. W. J., de Baere, E., Koenekoop, R. K., van Schooneveld, M. J., Strom, T. M., van Lith-Verhoeven, J. J. C., Lotery, A. J., van Moll-Ramirez, N., Leroy, B. P., van den Born, L. I., Hoyng, C. B., Cremers, F. P. M. & Klaver, C. C. W., 2009, In: American journal of human genetics. 85, 2, p. 240-247

    Research output: Contribution to journal › Article › Academic › peer-review

ID: 109643