Besides, the dry plate prepared in our laboratory from Nuclear Emulsion № 4.has also been tried, but only an incomplete outline was seen on the autoradiograph even after 124 days of exposure.

Na 125I labelled anti-Thy 1 antibodies and DNP-BSA were reacted separately with mouse lymph node lymphocytes and autoradiograph taken thereafter, so to identify the cell surface markers.

分别以~（125）碘化抗Thy1抗体及~（125）碘化DNP-BSA与小鼠淋巴结细胞相反应，然后进行放射自显影，从而初步建立了检测淋巴细胞表面标志的两种方法。

Automatic slide cytosedimentation machine subcellular autoradiograph

自动载物片细胞沉积机

The particulate-tracking autoradiograph ( PTA) technique is a powerful tool for studying the behaviors of boron in materials.

径迹显微技术（PTA）是研究硼的晶界偏聚的行之有效的方法。

The absorption and metabolism of γ-aminobutyric acid ( GABA) in rat were investigated by using 14 C autoradiograph and quantitative analysis method.

采用14C放射性自显影和化学定量法研究γ-氨基丁酸在白鼠体内的吸收和代谢。

The Application of Series of Super-HR Green Plates in Autoradiograph

Super HR系列感绿片在放射摄影中的应用

Establishment and Application of Autoradiograph Assay of p38 MAPK Activity

p~（38）丝裂原活化蛋白激酶活性放射自显影测定方法的建立和应用

The chromosomal breaks and fragments, univalents of auto-and sex-chromosomal type and translocation multivalents, especially a rare type, namely between an X chromosome and an autosome were increased at diakinesis-metaphase ⅰ.

在中期Ⅰ发现染色体断裂和断片、易位多价体、性染色体和常染色体的单价体频率显著增高。

The incidence rates of chromosome aberration cells, autosome univalent and sex chromosome univalent had no significant difference between the hexaflumuron-treated groups and the negative control ( P> 0.05) in the chromosome aberration test of primary spermatocyte of mice.

氟铃脲各剂量组的小鼠睾丸初级精母细胞染色体畸变细胞率、常染色体单价体发生率和性染色体单价体发生率与阴性对照组比较，差异无统计学意义（P>0.05）。

The reported ( abnormalities) included the numeric and structural abnormalities of X chromosome, 46, XY, 45, X0/ 46, XY, and the structural abnormality of autosome.

染色体异常包括X染色体数目及结构异常，46，XY、45，X0/46，XY以及常染色体结构异常。

Studies about the genetic diversity of Chinese domestic horses and donkeys were mainly concentrated on mitochondrial genome and autosome. Nevertheless, papers on genetic diversity and origins of Y chromosome in horse and donkey are limited.

目前有关中国马和驴品种遗传多样性的研究多数集中在线粒体DNA和常染色体DNA方面，对其Y染色体遗传多样性和起源进化的研究还比较缺乏。

Based on the hereditary properties of NPV resistance, a hypothesis was proposed and confirmed that the resistance is controlled by NN main gene on an autosome and Z+ Z+ minor genes on the sex chromosome.

根据其遗传规律的特殊性，提出常染色体上NN主基因和性染色体上Z+Z+修饰基因控制假设，并得到试验验证。

( 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；

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。

It has been shown that the numbers and the morphologies among the autosome pairs in these four breeds nearly coincided, but there were comparatively remarkable differences among the sex-chromosomes.

结果表明，这四个品种中常染色体对间的带纹数目及形态基本一致，而性染色体间的差异却较大。

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）；

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；

Of the 102 cases of oligospermia, 5 ( 4.9%) patients with the inversion and translocation of some fragments of autosome were identified.

102例少精子症病人中，检出异常染色体核型病人5例（4.9%），主要涉及常染色体某些片段的倒位、易位。

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%。

Sex development in human is determined by lots of genes on sex chromosomes and autosome. It can be divided into two stages: sex determination and sex differentiation.

人类性别发育包括性别决定和性别分化两个阶段，是由性染色体和常染色体上一系列性别决定和分化基因调控的。

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。