Figure 5 | Scientific Reports

Figure 5

From: Robust Preimplantation Genetic Testing of Huntington Disease by Combined Triplet-Primed PCR Analysis of the HTT CAG Repeat and Multi-Microsatellite Haplotyping

Figure 5

Results of clinical IVF PGT-M case. Electropherograms of (A) TP-PCR and (B) tridecaplex marker panel PCR are shown for the parental genomic DNAs, blastomere whole genome amplified DNAs, and fetal DNAs from the two successful pregnancies. Embryo 5 displayed the normal paternal haplotype only, while embryo 14 displayed both maternal haplotypes in addition to the affected paternal haplotype. AF, amplification failure; ADO, allele drop-out.

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