该病属常染色体隐性遗传，与X-染色体关联，所以，母亲是基因携带者的男性表现为发病。
The disease is autosomal-recessive and linked to the X-chromosome, so that men whose mothers are carriers of the gene manifest the disease.
因为布林先生最近发现，他从母亲那里遗传了一个变异的基因LRRK2。 研究显示，变异的LRRK2可能使得有家族患病史的携带者患帕金森氏症的几率增加。
The reason was that Mr Brin had recently discovered that he has inherited from his mother a mutation of a gene called LRRK2 that appears to predispose carriers to familial Parkinson’s.
通过遗传咨询门诊，对反复性流产患者夫妇双方或一方进行了染色体核型分析，共71例，检出平衡易位携带者3例。
The karyotypes cf 71 cases of recurrent abortion, or their couples were examined in genetic definition clinic, 3 cases of anomalous karyotype were observed.
这就表明隐形遗传疾病基因携带者可能还有过多的未知疾患。
That suggests that people who are recessive disease carriers could have more subtle disorders.
众所周知，DNA是遗传信息的携带者，遗传现象主要是由基因决定的。
As we all know, the heredity information is carried by DNA, and the hereditary phenomenon is determined mainly by genes.
目的：研究乙型肝炎表面抗原携带者及其子女间的遗传传递。
Objective: to study genetic transmission from the parents with HBsAg to their children.
目的：研究乙型肝炎表面抗原携带者及其子女间的遗传传递。
Objective: to study genetic transmission from the parents with HBsAg to their children.
应用推荐