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1. A birth of bipartite exon by intragenic deletion. Issue 3 (1st March 2017)

3. Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome. Issue 9 (30th July 2019)

5. Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndrome. Issue 2 (29th September 2021)

6. Improving survival in patients with trisomy 18. Issue 4 (8th December 2021)

7. Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay. Issue 8 (16th June 2020)

9. The utility of urinary CD80 as a diagnostic marker in patients with renal diseases. Issue 1 (December 2018)

10. The utility of urinary CD80 as a diagnostic marker in patients with renal diseases. Issue 1 (December 2018)