autosomal造句

• This disorder is inherited as an autosomal dominant trait .
  本病作为常染色体显性传递。
• Xeroderma pigmentosum is an autosomal recessive disease .
  着色性干皮病是一种常染色体的退行性疾病。
• Certain autosomal translocations in the heterozygous state can be fully viable .
  呈杂合子状态的某些常染色体易位完全可以生活的。
• An aneuploid state in which a third homologous chromosome is present in addition to the normal autosomal pair is called trisomy .
  除了正常染色体对以外，还存在有第二种同源染色体的非整倍体状态，被称为三体性。
• Autosomal recessive inheritance , ar
  常染色体隐性遗传
• Autosomal dominant inheritance ,
  常染色体显性遗传
• According to genetic analysis , this disease is caused by autosomal dominant inheritance
  经过遗传分析，认为该畸形属常染色体显性遗传。
• 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。
• This is tuberous sclerosis , an autosomal dominant condition characterized by mental retardation and seizures beginning early in life
  结节性硬化症，常染色体显性遗传，表现为智力低下、癫痫发作等。
• Complex vertebral malformation ( cvm ) , a lethal autosomal recessive inherited defect in holstein breed , was newly reported in demark
  摘要荷斯坦奶牛脊柱畸形综合征是近年新发现的一种常染色体隐性遗传病，该病对纯合子胎儿是致死性的。
• In the autosomal recessive condition , the parents are generally healthy ? we call them ‘ carriers . ’ the probability of them having a child with another affected child is 25 percent
  对于常染色体隐性遗传，父母表面上通常是正常的? ?我们称之为“携带者” 。他们生育相同疾病小孩的几率将是25 % 。
• Hemochromatosis can be primary ( the cause is probably an autosomal recessive genetic disease ) or secondary ( excess iron intake or absorption , liver disease , or numerous transfusions )
  血色素沉着症或可以是原发的（病因大概为常染色体隐性遗传病） ，也可以是继发的（过多的铁摄取或吸收、肝脏疾病、大量输血） 。
• Wilson " s disease is the consequence of toxic accumulation of copper initially in the liver and later in extrahepatic sites , this disorder is inherited in autosomal recessive manner and is present in 1 in 30000 individuals in all populations
  其中研究最多的是铜代谢异常所引起的wilson ' s病，这种病是常染色体隐性遗传病，如果肝脏中铜浓度达到毒性水平，将引发急性肝炎，其发生率为三万分之一。
• Nevoid basal cell carcinoma syndrome , also known as gorlin syndrome , is an autosomal dominant inherited disorder which is characterized by the presence of multiple maxillary keratocysts , facial basal cell carcinomas and kinds of musculo - skeletal disturbances
  摘要痣样基底细胞癌综合征是一种罕见的常染色体显性遗传疾病，以颌骨多发性角化囊肿，皮肤痣样基底细胞癌及多种骨骼异常为主要临床表现。
• Genomic imprinting refers to parent - of - origin - dependent gene expression . the presence of imprinted gene can cause cells with a full parental complement of functional autosomal genes to specifically express one allele but not the other , resulting in monoalielic expression of imprinted loci
  基因组印记是指一种依赖于亲本的基因表达形式，它导致常染色体上的功能基因单一表达一个等位基因而不表达另一个等位基因，造成印记位点的单等位基因表达。
• Now autosomal and y - chromosomal strs are widely researched and applied , while the x - str markers are not . because x chromosome has the character that the male transmits his x chromosome only to his daughter ( s ) , it can provide more information than the autosomal does , particularly in complex cases of kinship testing
  而在解决一些复杂的亲缘关系案件(如单亲父女关系的鉴定和缺乏双亲的姐妹亲缘关系的鉴定)时,由于父亲的x染色体具有只传给他的女儿(们)的遗传特性,因此在解决此类案件时有常染色体所无法比拟的优点。