autosomal

1. It is obviously autosomal dominant inheritance according to the pedigree.
   由于第一代病例仅为右眼虹膜缺损，故较支持中胚层迷走发育的理论。
2. Experimental research on preimplantation genetic diagnosis for autosomal dominant polycystic kidney disease
   常染色体显性多囊肾疾病行胚胎植入前遗传学诊断的实验研究
3. We report an infant delivered at31 weeks gestation with restrictive dermopathy, which is a rare autosomal recessive genodermatosis.
   我们报告一拘束性皮肤病变的31周出生婴儿，其为一罕见的，体隐性遗传皮肤病。
4. Progress in the gene-related study on autosomal retinitis pigmentosa
   常染色体遗传型视网膜色素变性相关基因的研究进展
5. High-resolution Ultrasonography in the Assessment of Autosomal Recessive Polycystic Kidney Disease
   高分辨率声呐部面仪高分辨超声在常染色体隐性遗传性多囊肾诊断中的价值
6. Application of the Number of Allele Shared among Autosomal STR Loci in Full Sibling Identification ( genetics) having dissimilar alleles at corresponding chromosomal loci.
   应用常染色体STR基因座共有等位基因数判别全同胞关系（遗传学）在相应的染色体位点上具有不同的等位基因。
7. Clinical genetics and gene mapping studies on a family with autosomal dominant congenital cataract
   常染色体显性遗传性白内障一家系的临床遗传学及基因定位研究
8. Conclusion The association of gap junction protein gene with this autosomal dominant congenital pulverulent cataract was preliminary excluded.
   我们在此研究的是一个不伴综合征的常染色体显性先天性粉尘状白内障家系。
9. Clinical Study of Laparoscopic Decortication Therapy for Patients with Autosomal Dominant Polycystic Kidney Disease
   经后腹腔镜肾囊肿去顶减压术治疗常染色体显性遗传性多囊肾
10. Clinical and pathological features of autosomal dominant inherited central core disease
    常染色体显性遗传性中央轴空病的临床表现和病理特点
11. Objective To elucidate the pathogenic genes in a pedigree with autosomal dominant ichthyosis vulgaris ( IV).
    目的研究一常染色体显性遗传寻常型鱼鳞病家系的致病基因。
12. Inversion heterozygotes are semi-sterile. Certain autosomal translocations in the heterozygous state can be fully viable.
    易位杂合体是半不育的。呈杂合子状态的某些常染色体易位完全可以生活的。
13. Wilson ′ s disease is a autosomal recessive inherited disease characteristic by metabolic disorder of copper.
    肝豆状核变性是一种铜代谢障碍的常染色体隐性遗传病。
14. Most mammals hae just two kinds of photopigment in their retinas: one is encoded in the X chromosome and the other in an autosomal ( non-sex) chromosome.
    大部分哺乳动物的视网膜中只有两种感光色素：一种编码在X染色体中另一种寸在于正染色体中。
15. It is a common occurrence in dogs and is thought to be a sex-limited autosomal recessive trait.
    该疾病常发于犬，并被认为具有限性常染色体隐性遗传特征。
16. Clinical and Basic Research on Autosomal Dominant Polycystic Kidney Disease Before and after Renal Transplantation
    肾移植前后常染色体显性遗传多囊肾的临床与基础研究
17. The condition is passed along genetically as an autosomal dominant trait.
    条件是家族的遗传作为常染色体显性遗传特征。
18. Missense mutation in the β B1-crystallin gene caused autosomal dominant congenital cataract in China
    晶状体蛋白βB1基因错义突变引起常染色体显性遗传性白内障
19. As with familial adenomatous polyposis, the inheritance pattern is autosomal dominant.
    家族性腺瘤息肉病的遗传方式是常染色体显性遗传。
20. Citrin deficiency is inherited in an autosomal recessive manner.
    希特林缺乏综合征是一种常染色体隐性遗传性疾病。
21. Objective: To observe the clinical effect of laparoscopic renal cyst decortication in patients with autosomal dominant polycystic kidney disease.
    目的：观察经后腹腔镜肾囊肿去顶减压术治疗常染色体显性遗传性多囊肾病的临床效果。
22. Paternity Index Calculation in Mutation Autosomal STR Locus
    常染色体STR突变基因座父权指数计算
23. Owing to the influence of various complex factors, it is possible for the heterozygote of autosomal dominant inheritance to appear in different phenotypes.
    由于各种复杂因素的影响，常染色体显性遗传的杂合子有可能出现不同的表现型，本文阐述了常染色体显性遗传的几种类型。
24. Haploid and autosomal variation within a linguistic continuum of the Uralic-speaking people of Eurasia.
    单倍体和常染色体显示欧亚大陆的乌拉尔语言为母语的人是连续的。
25. Recent research progress of pathogenic genes in autosomal dominant hereditary pulverulent cataracts
    常染色体显性遗传性粉尘状白内障致病基因的研究进展
26. Sex-limited autosomal dominant inheritance
    性限常染色体显性遗传；限性常染色体显性遗传
27. With pedigree analysis, the genetic mode of the disease in the family are autosomal dominant inheritance.
    据系谱分析，该疾病符合常染色体显性遗传方式。
28. We examined three families and suggest that it has an autosomal dominant trait with incomplete penetrance.
    我们研究了三个家庭，并表明，它有一种常染色体显性不完全外显。

adj

1. of or relating to an autosome
   1. autosomal gene