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通过染色体微阵列分析检测到分离和非分离的部透明度增加的胎儿的副本数量变异

Shuxian Huang1,2,3, Heming Wu2,3, Lingna She1,2,3

  • 1Department of Ultrasound, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.

Frontiers in genetics
|January 2, 2026
PubMed
概括

No abstract available in PubMed .

关键词:
染色体异常染色体微阵列分析复制号变种部透光度增加在产前诊断

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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