1q21.1微切除和微重复的产前诊断:一个回顾性的案例系列

Ziyang Liu1, Song Yi2, Manman Li2

  • 1College of Agronomy and Biotechnology, Southwest University, Chongqing, 400716, China.

Molecular cytogenetics
|October 1, 2025
PubMed
概括

产前1q21.1副本数变异 (CNVs) 显示不完全的透度和可变的表达性,没有特定的超声波标记. 父母对神经发育风险的焦虑影响了De novo CNVs的终止决定.

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