trisomy单词基本解析：

n.三（染色）体性，三（染色）体细胞
n. [生]三(染色)体性, 三(染色)体细胞
n.三（染色）体性，三（染色）体细胞；

trisomy变化用词：

trisomy英英释义：

Noun

1. chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell

名词 trisomy:

chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell

trisomy[ 'traisəumi ]n.chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell

trisomy中文词源：

trisomy用法和例句：

A short femur is associated with trisomy 21 rather than trisomy 13 and holoprosencephaly.

股骨短与21-三体而不是13-三体或全前脑畸形有关.

互联网

trisomy

*X represents monosomy 21,diploid,trisomy 21,tetrasonmy 21 and hexasomy 21 in the corresponding box.

(X代表相应栏中的21单体、二倍体、21三体、四体和六体)；

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。

10p partial trisomy syndrome

10p部分三体性综合征

10q partial trisomy syndrome

10q部分三体性综合征

trisomy 10

10三体综合征, 科凯恩综合征

Complete trisomy 10 syndrome

10完全三体性综合征

11p partial trisomy syndrome

11p部分三体性综合征

11q partial trisomy syndrome

11q部分三体性综合征

12p partial trisomy syndrome

12p部分三体性综合征

12q partial trisomy syndrome

12q部分三体性综合征

Six cases for trisomy 12 were detected by one centromeric probe for 12.And del(13q14.3),del(11q23) were usually detected in normal karyotype.

12号着丝粒探针检出6例有+12,而且D13S272(13q14.3)、ATM(11q23)缺失常发生在常规检测正常的核型。

trisomy 13 syndrome

13(号染色体)三体型综合征

13p partial trisomy syndrome

13p部分三体性综合征

13q partial trisomy syndrome

13q部分三体性综合征

trisomy 13

13三体

Complete trisomy 13 syndrome

13完全三体性综合征

14q partial proximal trisomy syndrome

14q近侧部分三体性综合征

14q partial distal trisomy syndrome

14q远侧部分三体性综合征

14q partial trisomy syndrome

14q部分三体性综合征

Complete trisomy 14 syndrome

14完全三体性综合征

15q partial trisomy syndrome

15q部分三体性综合征

16p partial trisomy syndrome

16p部分三体性综合征

16q partial trisomy syndrome

16q部分三体性综合征

trisomy 16

16三体

Complete trisomy 16 syndrome

16完全三体性综合征

trisomy syndrome 17-18

17-18三染色体综合征, E三染色体综合征:瘦弱、喂食困难、低位耳、颏后缩、精神呆滞、手足畸形

17p partial trisomy syndrome

17p部分三体性综合征

17q partial trisomy syndrome

17q部分三体性综合征

E trisomy

18-三体综合征

18p partial trisomy syndrome

18p部分三体性综合征

18q partial trisomy syndrome

18q部分三体性综合征

Complete trisomy 18 syndrome

18完全三体性综合征

19q partial trisomy syndrome

19q部分三体性综合征

1q partial trisomy syndrome

1q部分三体性染色体综合征

trisomy 20p syndrome

20P三体综合征

20p partial trisomy syndrome

20p部分三体性综合征

20q partial trisomy syndrome

20q部分三体性综合征

Complete trisomy 20 syndrome

20完全三体性综合征

trisomy 21 syndrome

21(号染色体)三体型综合征

Trisomy of chromosome21

21-三体

21q partial distal trisomy syndrome

21q远侧部分三体性综合征

21q partial trisomy syndrome

21q部分三体性综合征

trisomy 21

21三体

Keywords Trisomy 21;Aneuploid;In situ hybridization;Fluorescent;PGD;

21三体;非整倍体;高育龄;原位杂交;荧光;植入前诊断;

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

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。

Preclinical Study of Preimplantation Genetic Diagnosis of 21 Trisomy Syndrome

21三体综合症植入前诊断的临床前运用研究

Complete trisomy 21 syndrome

21完全三体性综合征

trisomy 22 syndrome

22(号染色体)三体型综合征

22q partial trisomy syndrome

22q部分三体性染色体综合征

Complete trisomy 22 syndrome

22完全三体性综合征

2p partial trisomy syndrome

2p部分三体性综合征

2q partial trisomy syndrome

2q部分三体性综合征

3p partial trisomy syndrome

3p部分三体性综合征

3q partial trisomy syndrome

3q部分三体性综合征

trisomy 4p syndrome

4P三体综合征(4号染色体短臂三体综合征)

4p partial trisomy syndrome

4p部分三体性综合征

4q partial trisomy syndrome

4q部分三体性综合征

trisomy 4

4号染色体三体

Trisomy for short arm of chromosome 4

4号染色体短臂三体性

5p partial trisomy syndrome

5p部分三体性综合征

Other common features of trisomy 13 include the holoprosencephaly complex with distinct facial features.(31,78) Forty percent of cases with trisomy 18 hae cleft lip with or without cleft palate.

60%的病例中，13三体与唇裂和腭裂或单纯腭裂密切相关，13三体常见的其他特征还包括前脑无裂畸形合并明显的面裂[31，78]。

6p partial trisomy syndrome

6p部分三体性综合征

6q partial trisomy syndrome

6q部分三体性综合征

7p partial trisomy syndrome

7p部分三体性综合征

7q partial trisomy syndrome

7q部分三体性综合征

trisomy 8 syndrome

8(号染色体)三体型综合征

8p partial trisomy syndrome

8p部分三体性综合征

8q partial trisomy syndrome

8q部分三体性综合征

Complete trisomy 8 syndrome

8号完全三体性综合征

trisomy 8

8号染色体三体

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

trisomy 9p syndrome

9P三体综合征, 9P三体性综合征

9p partial trisomy syndrome

9p部分三体性综合征

9q partial trisomy syndrome

9q部分三体性综合征

Complete trisomy 9 syndrome

9完全三体性综合征

trisomy C syndrome

C三体型综合征

D1 trisomy syndrome

D1三体性综合征

Cases of trisomy 21 were identified from the cytogenetics laboratory logbook.

Down综合征（21三体综合症）的鉴别参照细胞遗传学手册。

D trisomy syndrome

D三染色体综合征:脑、心脏、眼畸形, 有唇、腭裂及耳聋

用作名词(n.)

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。

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