常染色体

Giant parietal foramina can be an isolated entity or can be inherited in an autosomal dominant fashion.

巨顶骨孔可以是孤立发生的或常染色体显性遗传

Because TS is a genetic condition it can be passed on to a child.It is passed on in a way known as autosomal dominant.

因为6月24日ts是一种遗传条件，它可以通过对一个孩子，它是通过对在的方式称为常染色体显性遗传。

The apparent enlargement of the ventricles seen here is due to atrophy of the head of the caudate from neuronal loss with Huntington's disease, an autosomal dominant condition characterized clinically by choreiform movements.

明显的脑室扩张是因为Huntington病时二乙基溴乙酰胺丧失使尾状核头萎缩，常染色体显性遗传，临床上伴有典型的舞蹈症。

This report was to study the morphologic characteristics of dental and face in cleidocranial dysplasia.

锁骨颅骨发育不全综合征(C leidocranial dys-plia，CCD)是一种少见的常染色体显形遗传性疾病。

Hereditary porokeratosis is a disease of dominant autosomal heredity. The histopathologic characteristics is epidermic keratosis and comoid lamellae.

遗传性汗孔角化症是一种常染色体显性遗传病，以表皮明显角化、鸡眼样板作为其组织病理学特征。

2The involvement of MFT in woman is more than that in man.(3)The patients showed multiple dome-shaped, skin-colored, firm papules on the face. Some patients also present the lesions on the scalp and neck. No lesion showed the malignant tendency.(4) The histologic findings of MFT are cornified cysts and some nests of basaloid epithelial cells.(5)There were variable clinical expressions in different patients of the same family.(6) Some pedigrees were also affected by feckle or symmetrical progressive erythrokeratoderma, which were not found in MFT patients of other origin.

MFT临床分析总结：①MFT遗传方式为常染色体显性遗传；②女性发病多于男性；③中国汉族人MFT的典型皮损特征为面部乳白色半球形或圆锥形丘疹，质地坚实，只有2个家系皮损分别发生于头皮及颈部，均无恶化倾向；④组织病理特征为角质囊肿和由基底样瘤细胞构成的肿瘤岛；④同一家系中不同的患者表现度不同；⑤个别家系可伴发雀斑及进行性对称性红斑角化症，其它家系不伴发其他疾病。

To search the genetic heterogeneity of ADPKD and to compare the clinical presentation between ADPKD type 1 and 2 in Shanghai Han population, develop a method of gene diagnosis by linkage analysis with microsatellite DNA tightly linked to PKD1 and PKD2 and make gene diagnosis of mutation carriers before cystogenesis, detect single nucleotide polymorphism of PKD2 and its frequence in Han population.

根据知情同意的原则，选取80名无亲缘关系的上海市汉族健康志愿者进行与PKD1和PKD2连锁的微卫星DNA多态性的研究，选取43个常染色体显性多囊肾病家系进行遗传异质性、表型差异研究及基因诊断。

Dermoid sinus is a genetic, autosomal skin condition in dogs.

皮窦是一种犬类的常染色体遗传病。

Germ-line mutations in the genes hTERT and hTR, encoding telomerase reverse transcriptase and telomerase RNA, respectively, cause autosomal dominant dyskeratosis congenita, a rare hereditary disorder associated with premature death from aplastic anemia and pulmonary fibrosis.

分别编码端粒末端转移酶反转录酶和端粒酶RNA的hTERT和hTR基因的种系突变导致常染色体显性先天性角化不良，它是一种罕见的因为再生障碍性贫血和肺纤维化而早亡的遗传性疾病。

Germ-line mutations in the genes hTERT and hTR, encoding telomerase reverse transcriptase and telomerase RNA, respectively, cause autosomal dominant dyskeratosis congenita, a rare hereditary disorder associated with premature death from aplastic anemia and pulmonary fibrosis.

端粒酶逆转录酶的编码基因hTERT和端粒酶RNA的编码基因hTR发生种系突变时，可引起常染色体显性先天性角化不良，这是一种罕见的遗传性疾病，它与再生障碍性贫血和肺纤维变性所致的早产儿死亡具有相关性。

It has been put forward that there exists single Ball point and double Ball points on the symmetrical connecting-rod curves of equilateral mechanisms.

从鲍尔点的形成原理出发，分析对称连杆曲线上鲍尔点的产生条件，提出等边机构的对称连杆曲线上有单鲍尔点和双鲍尔点。

The factory affiliated to the Group primarily manufactures multiple-purpose pincers, baking kits, knives, scissors, kitchenware, gardening tools and beauty care kits as well as other hardware tools, the annual production value of which reaches US$ 30 million dollars.

集团所属工厂主要生产多用钳、烤具、刀具、剪刀、厨具、花园工具、美容套等五金产品，年生产总值3000万美元，产品价廉物美、选料上乘、质量保证，深受国内外客户的青睐