相关实验视频
Updated: Jul 15, 2026

FISH for Pre-implantation Genetic Diagnosis
Published on: February 23, 2011
艾曼纽尔综合征的产前诊断和咨询:两个病例报告
Chi-Yuan Chiang1, Zih-Ning Liu1, Shu-O Chiu2
1Department of Obstetrics and Gynecology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan.
艾曼纽尔综合征是一种罕见的遗传疾病,可以在产前检测到. 这项研究介绍了两个新的病例,并审查了其他病例,突出了转位异位生物的3:1分离导致这种情况.
科学领域:
- 遗传学 是一个遗传学.
- 产前诊断 在产前诊断
- 染色体异常 染色体异常
背景情况:
- 艾曼纽尔综合征是一种罕见的遗传染色体疾病.
- 它的特征在于由11·22转位的染色体22衍生出来的染色体22.
- 在亚洲人群中报告的病例很少.
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