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You searched for: Author/Creator Cremers, Frans P.M.

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1. A Post‐Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases. Issue 12 (18th October 2013)

5. Defining inclusion criteria and endpoints for clinical trials: a prospective cross‐sectional study in CRB1‐associated retinal dystrophies. Issue 3 (2nd February 2021)

6. Heterozygous Deep‐Intronic Variants and Deletions in ABCA4 in Persons with Retinal Dystrophies and One Exonic ABCA4 Variant. Issue 1 (January 2015)

8. Next Generation Genetic Testing for Retinitis Pigmentosa. Issue 8 (12th June 2013)

9. Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?. (April 2019)

10. Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype–Phenotype Correlations. Issue 1 (30th October 2013)