autosome

Cases were autosome abnormalities ( 4.00 % ) .

常染色体异常8例，检出率4.00%。

The numbers of MiHAs are huge and their coding genes are in the hole genome , including autosome , Y chromosome and mitochondrial gene .

MiHAs数量庞大，其编码基因分布于整个基因组，包括常染色体、Y染色体、线粒体DNA，现已发现的人类MiHAs有十几种。

44 cases ( 35 8 % ) were abnormal autosome .

44例（358%）为常染色体异常；

Model and Stability of Autosome Heredity

常染色体遗传模型及稳定性

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。

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。

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%。

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。

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；

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）；

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。

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。

( 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；

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。

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。

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。

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 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。