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Updated: Jun 29, 2025

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
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通过比较基因组杂交阵列检测男孩的4p16.3删除和11p15.5p15.4获取:一个案例报告

Işın Kaya1

  • 1Medical Genetics, Bakırçay University Çiğli Education ve Training Hospital, İzmir 35620, Turkey. isintkaya@yahoo.com.

World journal of clinical cases
|April 5, 2024
PubMed
概括

非基同源重组 (NAHR) 通过DNA复制数的变化引起基因组疾病. 这一案例突显了NAHR介导的儿童的删除和重复,导致基因组失衡.

关键词:
案例报告案例报告经常性的重新安排.银 - 拉塞尔综合征是什么?沃尔夫 - 希尔斯霍恩综合征是什么?

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