网络释义专业释义英英释义
遗传学超声检查胎儿常见的染色体三体的探讨_stmopen 关键词】: 遗传学超声;三体性;胎儿;超声检查 产前 [gap=827]Keywords】: Genetic ultrasound;Trisomy;Fetus;Ultrasonographyprenatal
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trisomy syndrome 三体综合征
trisomy 21 syndrome 小儿唐氏综合征
double trisomy 双三体
trisomy 13 syndrome 帕套综合征
trisomy X syndrome 综合征 ; X三体综合征
q partial trisomy syndrome q部分三体综合征
trisomy 8 三体
p partial trisomy syndrome p部分三体综合征
trisomy [ 'traisəumi ]
- n. chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell
以上来源于: WordNet
柯林斯英汉双解大词典
trisomy /ˈtraɪsəʊmɪ/
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1.
N the condition of having one chromosome of the set represented three times in an otherwise diploid organism, cell, etc. Trisomy of chromosome 21 results in Down's syndrome 三染色体性
双语例句权威例句
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In this paper, we report a case of X-trisomy, and analyse its mechanism and genetic effect.
本文报告一例单纯性x三体型，并对其发病机理和遗传效应进行了分析。
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Trisomy has been the focus of extensive medical research but the exact mechanism is still not understood.
三体综合症在医学研究上备受关注，但其确切机制仍未明确。
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This confirmed the presence of tetrasomy 8 and trisomy 8 and also revealed a low percentage of a pentasomy 8 clone.
这不但证实了三体8和四体8克隆的存在，还发现存在一个较小的五体8克隆。
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