2016-06-06 12:04
trisomy翻译
三体
音标读音
英式:['traɪsəʊmɪ]美式:['traɪˌsoʊmi:]
基本意思
n.三（染色）体性，三（染色）体细胞
形近的词
变形
例句
- Trisomy 7 and trisomy 12 are common chromosome aberrations in lymphoma.
+7和+12是淋巴瘤常见的染色体畸变。
- Amniocentesis was performed to rule out trisomy 21; the karyotype was normal: 46, XX.
羊水穿刺排除了21三体，染色体组型正常，46，XX。
- Objective To evaluate significance of prenatal ultrasonography in diagnosis of trisomy 18.
目的探讨超声在18-三体综合征产前诊断中的意义。
- Objective To assess the effectiveness of sonographic screening and discuss sonographic characteristics of Down syndrome and trisomy 18.
目的对21及18三体综合征胎儿的超声声像图特征和超声筛查的价值进行评估。
- Ultrasound screening for trisomy 21 syndrome at 11-13~ (+ 6) gestational weeks
超声在孕11-13~（+6）周筛查21-三体综合征中的作用
- A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.
作者报告一例具有多种先天性异常的三染色体22症的活产女婴。
- So this fetus presented seeral signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.
这样，本例胎儿显示21三体的若干征象：包括鼻骨发育不全、牙发育不全、小颌和尿道下裂。
- In 27 cases of 21 trisomy children and parents, the origin of extra 21 chromosomewas observated with chromosome analysis and G banding method.
本文对27例21三体儿童及其父母进行了染色体核型分析及G显带方法，观察其额外21号染色体来源。
- Impact of Trisomy 8 on Cytobiological and Clinical Features of Acute Myelomonocytic and Monocytic Leukemia
8号染色体三体对急性粒、单核细胞白血病细胞生物学和临床特征的影响
- Objective: A few trisomy 21 cells in normal chromosome karyotype was been observed for study of the correlation of clinical phenotype and development damage in sick children of Down's syndrome.
目的观察正常细胞核型中含有极少量21-三体细胞的患儿临床表型及发育损害的相关关系。
- The practical value with antenatal filtering examination to diagnosis trisomy syndrome
产前筛查在诊断18-三体综合征中的应用价值
- An aneuploid state in which a third homologous chromosome is present in addition to the normal autosomal pair is called trisomy.
除了正常染色体对以外，还存在有第二种同源染色体的非整倍体状态，被称为三体性。
- Study of Ag-stained NORS in Trisomy 21 Families
21三体征家庭的银染核仁形成区的研究
- The term GCD has been loosely used in the literature and many conditions with only occasional cortical cysts e.g. trisomy 13-15 and Zellweger's Syndrome, have been included < 2>.
“肾小球囊性肾病”已经被广泛的使用在文献和偶尔出现在皮质囊肿的病例中，这些病例包括13－15三体和脑肝肾综合征<2>。
- Establishment of a human embryonic stem cell line with trisomy 16
染色体16三体人胚胎干细胞系的建立
- A Simulation Study of the Abnormal EEG Morphology by the Numerical Method in a 3-D Space; Underlying chromosomal abnormalities, such as trisomy 13, or maternal diabetes mellitus are possible causes, but some cases are sporadic.
应用电场数值计算方法研究三维异常神经电活动正问题潜在的染色体异常，例如三倍体13，或母亲的糖尿病也是可能的原因。
- 21q partial distal trisomy syndrome
21q远侧部分三体性综合征
- One of the ideas that I am working on is that if a patient has trisomy 7 only we can give them an epidermal growth factor receptor inhibitor for six months and see if we can eradicate those clones.
在这方面我正在研究的一种思路就是，如果一个患者只有7三体，我们可以用表皮生长因子受体阻滞剂治疗6个月，观察是否能根除这种克隆。
- Underlying chromosomal abnormalities, such as trisomy 13, or maternal diabetes mellitus are possible causes, but some cases are sporadic.
潜在的染色体异常，例如三倍体13，或母亲的糖尿病也是可能的原因。
- Relative to fetuses with a nasal bone, those without a nasal bone were estimated to have about 150-times the risk of having trisomy 21.
与同有鼻骨的胎儿相比，那些没有鼻骨的胎儿估计有高于前者约150倍发生第21对染色体三体的机率。
- There is a weak but fairly convincing association between chromosomal abnormalities such as trisomy 21 ( Down syndrome) and echogenic foci in the heart.
在染色体异常（如21-三体）和心脏内强回声间有一定联系。
- 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。
- Hematological Characteristics and Prognosis of Myelodysplastic Syndrome with Sole Trisomy 11
单纯11三体骨髓增生异常综合征的血液学特征与预后
- First-trimester nuchal translucency, nasal bones, and trisomy 21 in selected and unselected populations
在挑选的和非挑选的人群中妊娠早期时的颈部半透明厚度、鼻骨及21-三体的关系
- Polysomy, which includes trisomy, is the condition in which one or more chromosomes are represented more than twice in the cell.
多染色体包括三染色体都是一条或多条染色体代替了正常细胞中的两条染色体形成的。
- In order to investigate the prevalence and distribution of trisomy 21 syndrome Down's syndron in China, an epidemiological study was conducted.
21三体综合征的现况研究旨在通过流行病学研究方法，了解中国21三体综合征的现患率及其分布特征。
- Object: To evaluate the prognostic impact of trisomy 8 on cytobiological and clinical features in acute myelomonocytic and monocytic leukemia ( M4, M5).
目的探讨8号染色体三体（8三体）对急性粒单、单核细胞白血病（M4、M5）细胞生物学及临床特征的影响。
- METHODS: Trisomy 16 mouse breeding;
方法：Trisomy16鼠培育；
- Objective: To improve the understanding and diagnostic ability of the brain changes in21 trisomy syndrome.
目的：提高对小儿21三体综合征脑部CT表现的认识和诊断。
- Meta-analysis of prenatal screening for trisomy 21 using nuchal translucency measurement with serum markers
血清学指标结合颈部透明膜产前筛查21-三体综合征的Meta分析
百科解释
网络意思