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According to the routine methods established by our center (Cai et al., 2020), cells from the villi, amniotic fluid, or umbilical cord blood samples of the 535 fetuses with CNS abnormalities were cultured, harvested, prepared, and G-banded. The prepared samples were collected and analyzed using the GSL-120 automatic chromosome scanning platform.
Copyright and License information: ©2021 Cai, Huang, Xu and Lin.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
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