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Fig. 3 | Thrombosis Journal

Fig. 3

From: 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 inversion

Fig. 3

Linked haplotype analysis of the HEMA F8 Inv22 PGT-M case. The high-risk marker haplotype of the carrier wife (in red) was established from the marker alleles present in the affected son. All three embryos inherited the maternal low-risk haplotype (in green) with no evidence of marker recombination, and are thus unaffected. ADO, allele dropout

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Thrombosis Journal

ISSN: 1477-9560

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