autosome

A disease caused by the presence of two recessive mutant genes on an autosome.

由于常染色体上出现突变基因而导致的疾病。

Both the Y and the X began to evolve from an autosome (a non-sex chromosome) some 300 million years ago.

大约三亿年前，Y与X染色体开始由体染色体（非关性别的染色体）逐渐演化。

The majority of the loci are at the autosome and five loci at the Z chromosome.Four loci have multiple allelic series.

这些基因座多数位于常染色体上，有5个基因座位于Z染色体上，有4个基因座存在有复等位基因系列。

Pedigree analysis reveals that it is consistent with autosome dominant inheritance.

用家系法分析, 符合常染色体显性遗传。

Twisting tongue is the recessive heredity of single gene of autosome , while the positive type is the recessive character.

翻舌为常染色体单基因隐性遗传,阳性为隐性性状。

A Holstein population with 2650 individuals was genotyped by 14 known microsatellite markers to map the QTL affecting milk production traits on BTA6 (Bos Taurus Autosome 6).

为了定位牛6号常染色体(BTA6,Bos Taurus Autosome 6)上影响产奶性状的QTL,分别利用了14个已知微卫星检测了2650头荷斯坦奶牛基因组样品的基因型。

Two congenital deaf and dumb pedigrees were reported,the hereditary model of two congenital deaf and dumb pedigree was autosome recessive heredity,which controlled by two pairs of genes.

报道了两个先天性聋哑家系.这两个家系中的先天性聋哑属常染色体隐性遗传，且有两对基因控制。

Abstract： Two congenital deaf and dumb pedigrees were reported,the hereditary model of two congenital deaf and dumb pedigree was autosome recessive heredity,which controlled by two pairs of genes.

摘 要： 报道了两个先天性聋哑家系.这两个家系中的先天性聋哑属常染色体隐性遗传，且有两对基因控制。

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.

Model and Stability of Autosome Heredity

常染色体遗传模型及稳定性

the autosome number the chromosome groups

常染色体分组序号

the chromosome groups, the autosome number

常染色体分组序号

Keywords Autosome;Polymorphism;Male infertility;

常染色体;多态性;男性不育;

autosome dominant inheritance(AD)

常染色体显性遗传

a disease caused by a dominant mutant gene on an autosome

由于常染色体突变基因导致的疾病

a disease caused by a dominant mutant gene on an autosome.

由于常染色体突变基因导致的疾

Keywords retinitis pigmentosa;autosome dominant;linkage analysis;

关键词视网膜色素变性;显性遗传;连锁分析;

autosome dominant inheritance

AD

autosome recessive inheritance

常染色体隐性遗传

Keywords Sparse mouse;Hairless mouse;Inbred strain;Backcross;Autosome;

关键词稀毛鼠;裸鼠;近交系;回交;常染色体;

Clinicopathological study on cerebral autosome dominant arteriopathy with subcortical infarcts and leukoencephalopathy

伴有皮层下梗死和白质脑病的常染色体显性遗传性脑动脉病临床病理研究

Keywords Congenital fibrosis of extraocular muscles;Autosome dominant;Linkage analysis;KIF21A gene;

先天性广泛眼外肌纤维化综合征;显性遗传;连锁分析;Kif21A基因;

Keywords eupolyphaga seu steleophaga;kidney;polycystic;autosom al recessive;epithelium;

土鳖虫;肾;多囊;常染色体显性;上皮细胞;

Keywords hearing impairment;autosome recessive inheritance;SLC26A4 gene;denaturing high performance liquid chromatography （DHPLC）;mutation;molecular epidemiology;

耳聋;常染色体隐性遗传;SLC26A4基因;变性高效液相色谱（DHPLC）;基因突变;分子流行病学;

haploid set of autosome

单套常染色体

autosome

n. 常染色体, 正染色体

autosome dominant

常染色体显性遗传

autosome dominant disease

常染色体显性遗传疾病

autosome loss

常染色体丢失

autosome recessive

AR

autosome recessive disease

常染色体隐性遗传病

autosome recessive(AR)

常染色体隐性遗传

autosome(enchromosome)

常染色体, 常染色体单倍体组