trisomy

trisomy

美 　英 ['tra?s??m?]

  • n.〔遺〕三體性；三體型
  • 網絡三染色體；三性體；染色體增加

英漢解釋

n.
1.
〔遺〕三體性
2.
三體型

英英解釋

n.

例句

An aneuploid state in which a third homologous chromosome is present in addition to the normal autosomal pair is called trisomy.

除了正常染色體對以外，還存在有第二種同源染色體的非整倍體狀態，被稱為三體性。

This is the heart of a premature stillborn with Trisomy 13 in which a ventricular septal defect is visible in the membranous septum.

這是一例因13三體綜合征而流產的早產兒心臟。可見室間隔缺損。

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.

與同有鼻骨的胎兒相比，那些沒有鼻骨的胎兒估計有高于前者約150倍發生第21對染色體三體的機率。

Trisomy has been the focus of extensive medical research but the exact mechanism is still not understood.

三體綜合癥在醫學研究上備受關注，但其確切機制仍未明確。

So this fetus presented several signs of trisomy 21, including the hypoplasia of the nasal bone, hypodontia, micrognathia, and hypospadias.

這樣，本例胎兒顯示21三體的若干征象：包括鼻骨發育不全、牙發育不全、小頜和尿道下裂。

Derivation of a formula for determination of proportion of paternal trisomy 21 is presented.

推導公式確定比例的父親是21三體。

Autosomal trisomy is a common cause of human miscarriage, malformations and learning disability.

常染色體是人類的共同事業流產，畸形和學習障礙。

A case of partial trisomy 13 is found on a male baby aged 3 months with multiple congenital abnormalities.

本篇報告一例第13對部分三染色體之3個月大男嬰，病人自出生卽被發現有多方面的先天性異常；

Symmetrical clavicular widening was observed in a boy with mosaic trisomy for chromosome 8.

對稱鎖骨擴大觀察一個男孩花葉為8號染色體三體。

A case of trisomy 22 liveborn female baby with multiple congenital anomalies is described.

作者報告一例具有多種先天性異常的三染色體22癥的活產女嬰。

Objective To evaluate significance of prenatal ultrasonography in diagnosis of trisomy 18.

目的探討超聲在18-三體綜合征產前診斷中的意義。

Down syndrome (trisomy 21) is a disorder caused by the presence of an extra 21st chromosome.

唐氏綜合癥（21三體綜合癥）是由于患者額外多了一條21號染色體所致的疾病。

Underlying chromosomal abnormalities, such as trisomy 13, or maternal diabetes mellitus are possible causes, but some cases are sporadic.

潛在的染色體異常，例如三倍體13，或母親的糖尿病也是可能的原因。

Cases of trisomy 22 usually present with many severe malformations, and they rarely survive to term.

三染色體22癥會引起嚴重的先天性畸形，因此活產病例相當少見。

Down's syndrome or trisomy 21 occurs in around 1 in 800 births and older women are at higher risk.

唐氏綜合癥又稱21三體綜合癥，發生率大約在八百分之一，產婦年齡越大，發病率越高。

Comparison of Detection of Trisomy 8 with Fluorescence In Situ Hybridization and Conventional Karyotype Analysis in Myelodysplastic Syndrome

熒光原位雜交和常規核型分析檢測骨髓增生異常綜合征8號染色體三體的比較

Genetic ultrasound: diagnostic value in detection of the trisomy in fetuses

遺傳學超聲檢查胎兒常見的染色體三體的探討

Comparative Histomorphological Study on the Craniomaxillary Development of the Trisomy-18 with Cleft Palate and Euploid Mice

18三體腭裂小鼠顱上頜復合體發育的比較組織形態學研究

Impact of Trisomy 8 on Cytobiological and Clinical Features of Acute Myelomonocytic and Monocytic Leukemia

8號染色體三體對急性粒、單核細胞白血病細胞生物學和臨床特征的影響

Rapid detected of trisomy 21 syndrome by gene diagnosis techniques

快速檢測21三體綜合征基因診斷方法的研究

The use of the primed in situ labeling technique in the diagnosis of 21-trisomy syndrome

引物原位標記技術在21-三體綜合征診斷中的應用

Morphometrical study on the development of the trisomy-18 with cleft palate and euploid mice

18三體腭裂小鼠顱頜面發育畸形的形態測量學研究

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