Fig. 2From: Robust preimplantation genetic testing of the common F8 Inv22 pathogenic variant of severe hemophilia A using a highly polymorphic multi-marker panel encompassing the paracentric inversionElectropherogram results from the HEMA F8 Inv22 PGT-M case, after single-tube multiplex-PCR of 13 F8-associated STR markers and the sex chromosome discriminating AMELX/Y marker. Results of the couple and their affected son were generated from peripheral blood DNA, while the embryo results were generated from trophectoderm biopsies. ADO, allele dropoutBack to article page