这是关于癌症的一个很新的领域。在过去的十年里,人们对于遗传学和人类基因组的理解已经到达这样的一种境界,那就是可以在临床利用这些信息,尤其是试图去了解癌症高发或者有高发倾向的家庭所遇到的严重的基因问题。
This is really an incredibly new area in terms of dealing with cancer. Over just the last 10 years, our understanding of genetics and of the humans genome has gotten to the point where clinically we can actually use this information in some situations, particularly to try to identify the underlined genetic problems in families that have a very high predisposition to cancer or very high incidents of cancer.
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