Skip to content

1 paper indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Open access Nov 2026

Comprehensive prospective investigation of splicing variants in the coding region of RHD: Insights into phenotypic consequences including revision of RHD*weak D type 3.

The functional effect of the RHD weak D type 3 allele is redefined and the combination of computational and experimental analyses is instrumental for rare variant interpretation and genotype-phenotype correlation studies.

Y. Fichou, C. Tournamille, G. Thomas et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.