Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode.
摘要牙本质形成不良是一种体染色体显性遗传的中胚层缺陷。
| 单词 | autosomal dominant |
| 例句 |
英语例句库
Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode. 摘要牙本质形成不良是一种体染色体显性遗传的中胚层缺陷。 Conclusion: The genetics of the true pattern in human palmar hypothenar area may belong to autosomal dominant inheritance. 手掌小鱼际区真实花纹可能属于常染色体显性遗传。 Congenital microphthalmia is a developmental defect of ocular disorder with autosomal dominant, autosomal recessive, and X-linked recessive modes of inheritance. 先天性小眼球是一种先天发育异常性眼科疾病,遗传方式有常染色体显性遗传、常染色体隐性遗传和X连锁隐性遗传。 声明：以上例句、词性分类均由互联网资源自动生成，部分未经过人工审核，其表达内容亦不代表本软件的观点；若发现问题，欢迎向我们指正。
原声例句
Osmosis-神经 Many different types have been identified most of which are autosomal dominant. 目前已经鉴定出许多不同的类型，其中大多数是常染色体显性的遗传模式。 日常生活医学科普 Causes It is mostly inherited as " autosomal dominant" pattern so patients have positive family history. 原因多为常染色体显性遗传，患者有阳性家族史。 Osmosis-生殖 Mutations in BRCA-1 or BRCA-2 are both autosomal dominant mutations, which can be inherited and cause familial breast cancer. BRCA-1和BRCA-2的突变都是常染色体显性突变，可被遗传并导致家族性乳腺癌。 Osmosis-血液肿瘤 There are two types of familial, or congenital, protein C and S deficiency; both are inherited in an autosomal dominant manner. 家族性（先天性）蛋白C和S缺乏症有两种，均为常染色体显性遗传。 Osmosis-神经 Individuals with tuberous sclerosis have a mutation in either the gene TSC1 or TSC2, and these mutations have an autosomal dominant inheritance pattern. 结节性硬化症患者的TSC1或TSC2基因发生了突变，为常染色体显性遗传。 Osmosis-血液肿瘤 All right, as a quick recap, acute intermittent porphyria is an autosomal dominant disorder caused by a deficiency of the enzyme porphobilinogen deaminase in the heme synthesis pathway. 好，快速回顾一下：急性间歇性卟啉病是常染色体显性疾病，由血红素合成途径中缺乏卟胆原脱氨酶导致。 Osmosis-神经 Now most of these gene mutations are inherited in an autosomal dominant pattern, meaning that one copy of an altered SCA gene is enough to cause the disease. 大多数的突变都以常染色体显性模式遗传，这代表一个SCA基因突变的拷贝足以引起这种疾病。 Osmosis-生殖 There are also genetic risk factors like having the BRCA-1 or BRCA-2 mutation, which are both autosomal dominant mutations, which in addition to ovarian cancer, carry with them an increased risk of breast cancer. 还有遗传相关的风险因素，如BRCA-1和BRCA-2突变，它们都是常染色体显性突变；除了卵巢癌之外，携带它们也会增加乳腺癌患病风险。 Osmosis-遗传 It's autosomal dominant, which means that even if there's a normal copy of the gene, a single mutated copy of the gene – in other words a heterozygous mutation - is sufficient to cause the disease. 这是一种常染色体显性遗传病，这意味着即使有一个正常基因，只要染色体上有一个突变的基因，即杂合突变，就足以致病。 |
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