https://taarsignals.com/index.....php/concurrent-raise
This is the first report of a unique phenotype, which can be secondary to a microdeletion encompassing TRIP12 and NPPC.No genetic relationship with recurrent pregnancy loss (RPL) due to embryonic aneuploidy was discovered. Recent research reports have suggested that the typical genetic variant rs2305957, surrounding the PLK4 gene, contributes to mitotic-origin aneuploidy risk during human being early embryo development. The
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