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。

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Automatic slide cytosedimentation machine subcellular autoradiograph

自动载物片细胞沉积机

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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。

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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。

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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

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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

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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。

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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）。

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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。

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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。

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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。

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( 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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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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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。

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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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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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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。

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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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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。

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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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