Fig. 1From: 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 inversionStructure of chromosome X band q28 between F8 and the telomere. Top line depicts a normal F8 allele, while bottom line depicts a pathogenic F8 Inv22 allele. Positions of 13 STR markers spanning and flanking the inversion interval are shownBack to article page