1、

Forcron could decrease the mitotic index and lead to various types of chromosome aberration.

异丙莠能降低蚕豆根尖细胞有丝分裂指数并诱导染色体产生多种类型的畸变.

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2、

Cases were autosome abnormalities ( 4.00%).

常染色体异常8例,检出率4.00%。

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3、

44 cases ( 35 8%) were abnormal autosome.

44例(358%)为常染色体异常;

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4、

Model and Stability of Autosome Heredity

常染色体遗传模型及稳定性

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5、

Pedigree analysis suggests that FASD is a autosome dominant heredity disease.

家谱分析显示,遗传方式符合常染色体显性遗传。

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6、

And there are 34 cases of autosome abnormalities which is 25% in all examiners and 46% in chromosome abnormalities.

常染色体异常34例,占全部被检者25%,占异常核型46%。

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7、

The hereditary mode of handedness or folding leg was likely the dominant heredity of single gene of autosome, and the right type of them was the dominant character.

利手和叠腿很可能均为常染色体单基因遗传,利手右型和叠腿右型分别为显性性状;

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8、

The segregative rate in generalized anxiety disorder was 0.225, which was not significantly different ( P> 0.05) from the segregation rate 0.25 in autosome recessive inheritance.

广泛性焦虑校正分离率为0.225,与常染色体隐性遗传的分离率0.25相比较,差异无显著性(P>0.05);

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9、

It is a recessive hereditary disease of autosome to be deaf and dumb. It was analysed through heredity that reducing or preventing consanguineous marriage can reduce the deaf-mute's birth rate.

聋哑是常染色体隐性遗传病,通过遗传分析发现,减少或防止近亲结婚可以降低聋哑人的出生。

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10、

( 2) The hereditary mode of rolling tongue or pointed tongue was the dominant heredity of single gene of autosome, and the can-rolling type or can-pointed type was the dominant character.

卷舌和尖舌均为常染色体单基因显性遗传,能卷舌型和能尖舌型分别为显性性状;

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11、

In a consecutive series of 12 autopsied cases ( 15 to 34 yrs) of accidental death in Nanning, desmin-positive intimal smooth muscle cells ( SMC) of the aortae and coronary arteries were found by immunohistochemistry.

连续12例意外死亡的广西自治区南宁市年轻人(15~34岁)免疫组化染色证明,其主动脉及冠状动脉内膜的平滑肌细胞含有较多结蛋白。

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12、

Prepare paraffin section of the line HE staining of each group of mice auricles to observe the histological differences and the changes of the auricle epidermis thickness and total thickness of mice auricle with microscope. Results: 1.

制作各组小鼠耳廓的石蜡组织切片行HE染色,并在显微镜下比较各组组织学变化及各组耳廓表皮厚度和总厚度的变化。

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14、

125 RA and 159 CTD of Serum RF, ATK levels were measured by the nephelometry quantitative and immunolabelling technique qualitative.

方法对125例RA和159例结缔组织病患者(CTD)采用散射比浊定量与荧光染色法测定RF与AKA。

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15、

Results In the 6 unrelated families of PD patients, 1 case had exon 5 deletion, its hereditary manner was autosomal recessive inheritance, the patient's age at the onset was 60 years old, clinical feature was tremor, rigidity and bradykinesia, but no athetosis.

结果6例患者中,发现1例有第5外显子缺失,其遗传模式呈常染色体隐性遗传,起病年龄60岁,临床表现为震颤、僵直和运动迟缓,但无异动症。

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16、

Methods: Radioimmunoassay ( RIA) and Wright Giemsa stain were used to detect serum sexual hormone and sperm cytology in 45 aspermia patients.

方法:45例无精子症病人采用放射免疫法(RIA)检测性激素,瑞吉染色法进行精液细胞学检查。

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17、

This paper studied the spray dying technology of ethylparaben microencapsulation. The result showed that the wall materials and their suitable proportion was Arabic gum 25%, Aperture starch 25%, and corn syrup 50%.

研究了利用喷雾干燥法制取微胶囊型尼泊金丙酯的工艺技术,结果表明:壁材及组分的最佳比例为:阿拉伯胶5%,微孔淀粉25%,玉米糖浆50%;革兰氏染色阴性;

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18、

Greedy algorithm is a simple approximative method in graph coloring.

贪心算法用于图的染色问题是一种简单的近似方法。

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19、

The value of APM histochemical stain technique in the diagnosis of amniotic fluid embolism

APM染色法在羊水栓塞诊断中的应用价值

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20、

In this paper two patients of antitype stigma has been reported by using G banding techniques of chromosomes and chromosomes in situ hybridization.

本文报告了2例临床症状不典型而用G带分析和染色体原位杂交证实了的该综合征患儿。

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