"Autosomal dominant inheritance"是指常染色体显性遗传，是一种遗传方式，意味着如果一个基因位于常染色体上，并且这个基因的存在会导致某种特征或疾病的表现，那么这个特征或疾病就有可能通过显性方式遗传给后代，即只要有一个携带者（携带该基因的人），其后代就有可能患上该特征或疾病。
以下是一篇关于常染色体显性遗传的英文范文：
Autosomal Dominant Inheritance
Autosomal dominant inheritance refers to a type of genetic inheritance in which a trait or disease is passed down from one generation to the next through an autosomal gene. If an autosomal gene carries a mutation that causes a particular characteristic or disease, it will be expressed in the next generation if it is inherited in an autosomal dominant manner. This means that as long as one person in the family carries the mutated gene, there is a chance that their offspring will inherit the trait or disease.
This type of inheritance is common in many inherited diseases and conditions, including Huntington's disease, myotonic dystrophy, and some forms of blindness and deafness. Understanding the genetics of autosomal dominant inheritance can be helpful for individuals and families who are at risk for inheriting a particular trait or disease, as it can help them to make informed decisions about their health and family planning.
"Autosomal dominant inheritance"是指一种遗传方式，其中遗传性状或疾病通过一对等位基因的显性基因在染色体上传递给后代。这意味着如果父母中的一个携带这种基因，他们的孩子有可能会出现这种症状，而另一个孩子则可能不会出现。这种遗传方式通常涉及单个染色体上的基因，并且通常在人类中表现为单基因遗传。
以下是一篇关于Autosomal Dominant Inheritance的英文范文：
Autosomal Dominant Inheritance: A Common Genetic Pattern
Autosomal dominant inheritance is a common pattern in genetics, where a trait or disease is passed down from one parent to their child through a single dominant gene on one of the twenty autosomes (non-sex chromosomes). If one parent carries the gene, there is a chance that their child may inherit it and develop the trait or disease, while the other child may not carry the gene and be unaffected. This pattern is often seen in conditions such as Huntington's disease, cystic fibrosis, and many others.
了解更多相关信息，请查询相关文献或咨询专业人士。
“常染色体显性遗传”（autosomal dominant inheritance）是一种遗传方式，指的是一种基因缺陷通过常染色体遗传给后代，其中缺陷基因只需要一个就可以导致疾病的表现。这种遗传方式的特点是，如果一个携带者与没有该缺陷的人结婚并生育孩子，孩子有50%的可能性携带缺陷基因。
至于“autosomal dominant inheritance英文范文最新变化”，这可能意味着关于常染色体显性遗传的英文文章或报告的更新或修改。然而，我无法提供具体的范文，因为我没有实际阅读过最新的英文范文。你可以在相关的生物学、遗传学或医学研究文献中寻找这方面的最新资料。