https://phosphorylasesignals.c....om/index.php/going-e
Fetuses with unusual karyotyping or CMA results were omitted. We performed WES on DNA samples from qualified fetus-parental trios and identified diagnostic hereditary alternatives predicated on ultrasonographic features. Results A total of 163 eligible fetus-parental trios had been successfully reviewed by WES. We found 26 likely pathogenic or pathogenic variants in 18 genetics from 20 fetuses, with an overall total proport
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