7p22.2 微复制:一种致病性CNV?
Alessia Bauleo1, Alberto Montesanto2, Vincenza Pace1
1BIOGENET, Medical and Forensic Genetics Laboratory, 87100 Cosenza, Italy.
Genes
|June 28, 2023
概括
染色体7p22.2中的微重复与神经发育障碍有关. 这项研究详细介绍了两个病例,将它们与7p22.1微复制综合征区分开来,并突出了7p22.2的作用.
科学领域:
- 遗传学 是一个遗传学.
- 人类遗传学 人类遗传学
- 分子遗传学 分子遗传学
背景情况:
- 染色体7短臂 (7p) 的部分重复是一种罕见的染色体重新排列,具有可变的表型.
- 高分辨率微阵列技术已经确定了7p22.1子频段是导致7p22.1微复制综合征的原因.
关键词:
7p2222第七部分7p22.2 微复制的微复制在CNV中,CNV是NV.SDK11是SDK11的第一个版本.阵列-CGH. 这是. 7p22.12.1第七部分 其他最小的关键区域是最小的关键区域.神经发育现象型的神经发育现象型更多相关视频
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