三染色体的

In this paper,the comparative studies on the effects of triazine herbicide Atrazine on seedlings growth,contents of chlorophyll and soluble protein,chromosome structure of root meristem,protein compositions of root meristems and chloroplast have been made in Oryza sativa.

比较研究了不同浓度三氮苯类除草剂对水稻幼苗生长、叶绿素及可溶性蛋白质含量、根尖分生组织染色体结构、分生组织和叶绿体蛋白质组分的影响。

For investigating the linkage group to which the semidwarf gene sd-t belongs,the crosses between Aitaiyin 2(ATY2),a variety of sd-t carrier in indica rice,and marker stocks as well as the trisomic lines of IR36 were made.

以籼型标志基因系和IR36三体为工具材料，通过杂交研究了籼稻矮秆材料矮泰引-2所携半矮秆基因sd-t在染色体上的位置。

For investigating the linkage group to which the semidwarf gene sdn belongs, the cross between Yizhi\|lashuangai, a material of sdn carrier of Indica rice, and marker stocks as well as the trisomic lines of IR36 were made.

以籼型标志基因系和IR3 6三体为工具材料，通过杂交研究籼稻矮秆材料一枝腊双矮所携半矮秆基因sdn在染色体上的位置。

Trisomy 21 is the existence of the third copy of the

但是为了不引起混乱，将第21对与第22对的名称对调，现在继续沿用"第21对染色体三体变异"这一名称。

It turned out that 7 cases were found with trisomy 21.4 cases among the 9916 negative-screening cases were born with trisomy 21, according to the analysis of the chromosome karyotypes in peripheral blood.

在筛查阴性的9916例中，出生DS患儿4例，经外周血染色体核型分析证实为21三体。

Methods To analyze retrospectively the ultrasonography of 8 cases which had been karyotyped to be trisomy 18 by fetal blood sampling or amniocentesis.

对脐血或羊水染色体核型分析确诊为18三体综合征的8例胎儿超声声像图进行回顾性分析。

It was original report to find the developmental delay of the ENS, absence of submucosal plexus and the aganglionic segment of colon ending in trisomy 16 mice, an animal model for Down syndrome.

Down综合征的动物模型常染色体16三体胎鼠ENS发育迟缓，粘膜下神经丛发育障碍出现后肠末端无神经节区。

Refers to Down's syndrome (Down's syndrome, dementia-like伸舌) screening, that is, pumping blood or amniotic fluid do villus cells, and then do Karyotype analysis, such as the emergence of 21 - trisomy map, you can diagnose fetus for Down syndrome. 2, AFP Chinese name for the AFP, such as maternal and fetal amniotic fluid were increased AFP confirmed fetal neural tube defects, namely spina bifida, spinal Meningocele, no brains infants, microcephaly, hydrocephalus.

是指唐氏综合症的筛查，就是抽绒毛血或羊水做细胞培养，然后做染色体核型分析，如出现21-三体综合征图谱，即可诊断胎儿为唐氏综合征。2、AFP中文名称为甲胎蛋白，如母血及胎儿羊水AFP均增高，证实胎儿有神经管畸形，即脊柱裂、脊脑膜膨出、无脑儿、小头畸形、脑积水。

To study the AgNORs correlation between lymphocyte chromosomes and lung cancer ceils in 3 type lung cancer patients.

目的 探讨三型肺癌患者淋巴细胞染色体和癌组织AgNORs的相关性。

Investigation in 308 family trios suggested a co-dominant X-linked inheritance and mutations were not found.

对308个三联体的家系调查表明这两个基因座符合X染色体共显性遗传，未发现突变。

And Pharaoh spoke to Joseph, saying, Your father and your brothers have come to you.

47：5 法老对约瑟说，你父亲和你弟兄们到你这里来了。

Additionally, the approximate flattening of surface strip using lines linking midpoints on perpendicular lines between geodesic curves and the unconditional extreme value method are discussed.

提出了用测地线方程、曲面上两点间短程线来计算膜结构曲面测地线的方法，同时，采用测地线间垂线的中点连线和用无约束极值法进行空间条状曲面近似展开的分析。