常染色体

The progressive muscular dystrophy is the human phenotype blemish caused by injured DNA. It is compatible with an autosomal dominant inheritance and it has penetrance and expressivity.

结论进行性肌营养不良是由DNA损伤引起的人类表型缺陷；该病症符合常染色体显性遗传；该病的发生具有一定的外显率和表现度。

Five percent individuals at each tail of the whole population were selected to establish two extrem groups for Haugh Unit and shell strength, and standard ...

位于常染色体上的17个标记的平均多态信息含量为0.44平均杂合度为0.497，从分子水平上证明经过10年的育种，矮小型蛋鸡群体的纯合度达到了很高的水平。

It contains the largest autosomal block of heterochromatin, which is heteromorphic in 6–8% of humans, whereas pericentric inversions occur in more than 1% of the population.

它具有最大的常染色体异染色质区域，其在6-8％的人群中为异型的，然而中心周围倒位在人群中出现率大于1％。

These populations are of particular research value homozygosity mapping of autosomal recessive mendelian diseases and in the establishment of extended haplotypes for understanding the genetic component of common diseases.

这些特殊的人群对于研究常染色体隐性遗传疾病的同源性作图，并进一步建立单倍型模式来研究常见病的遗传机制都具有极大的价值。而当今的土耳其已经具备一流的高等学府和临床教学机构来充分利用这些资源。

Joubert syndrome is an autosomal-recessive disorder, characterized by clinical presentation of hypotonia, ataxia, and global developmental delay.

jouber综合症是一种常染色体遗传性病变，临床表现为张力减低、共济失调、大脑半球发育延迟。

Disseminated superficial actinic porokeratosis is an uncommon autosomal dominant chronic keratinization disorder, characterized by multiple superficial keratotic lesions surrounded by a slightly raised keratotic border.

播散性浅表性光线性汗孔角化症是一种以多个浅表的角化性皮损，边缘轻微嵴状角化性隆起为特征的少见的慢性角化性皮肤病，呈常染色体显性遗传。

There is an agreement that autosomal recessive juvenile parkinsonism is a monogenic disease caused by mutation in parkin gene.

一致的观念认为常染色体隐性遗传性青少年型帕金森综合症是parkin基因突变引起的一种单基因遗传病。

The sparse character is autosomal recessive inheritance which is controlled by monogenic, and its heredity rule is completely consistent with Mendelian inheritance.

KM鼠稀毛性状，是受单基因控制的常染色体隐性遗传。其遗传规律完全符孟德尔的独立分离定律。

A rare exception is the KE family, a large three-generation pedigree in which approximately half of the members are affected with a severe speech and language disorder which appears to be transmitted as an autosomal dominant monogenic trait.

一个罕见的例外是KE家族，一个庞大的三个世代的谱系，其中将近半数的成员受到严重的言说和语言失调的影响，显示受到以此种遗传作为常染色体显性单的基因起源特徵。

Objective To study the location of disease related gene in a hereditary spastic paraplegia family with autosomal dominant inheritance in Tibet.

目的对西藏地区的一个常染色体显性遗传的家族性痉挛性截瘫家系的致病基因进行定位研究。

With Death guitarist Schuldiner adopting vocal duties, the band made a major impact on the scene.

随着死亡的吉他手Schuldiner接受主唱的职务，乐队在现实中树立了重要的影响。

But he could still end up breakfasting on Swiss-government issue muesli because all six are accused of nicking around 45 million pounds they should have paid to FIFA.

不过他最后仍有可能沦为瑞士政府&议事餐桌&上的一道早餐，因为这所有六个人都被指控把本应支付给国际足联的大约4500万英镑骗了个精光。