Such adaptations include gene mutations that shift the way penguins see the world.

适应包括改企鹅看世界的方式的基。

Finally, the diagnosis is confirmed by genetic testing to look for hemoglobin gene mutations.

最后，可以通过基检测寻找异常血红蛋白基进行确诊。

Genetic tests for known gene mutation associated with Kallmann syndrome can also be done.

也可对已知与Kallmann综合征相关的基进行基检测。

In addition, there are new genetic technologies on the horizon aimed at correcting specific gene mutations.

此外，还可以预见新的基治疗手段通过纠正特定来治疗疾病。

Based on research of white and brown coast pandas, this could be due to a gene mutation.

“根据对白熊和棕熊的研究，可能是基。

The majority of individuals with the HMBS gene mutation and a deficiency of porphobilinogen deaminase are asymptomatic.

存在HMBS基及缺乏卟原脱氨酶的人群大部分没有症状。

An inquiry into her case found they could have died of natural causes because of incredibly rare gene mutations.

对她的案件的调查发现，她的孩子们可能是为极其罕见的基，属于自然死亡。

She tested negative for the BRCA1 and BRCA2 gene mutation that increases a woman's risk of breast and ovarian cancer.

她的BRCA1和BRCA2基检测呈阴性，基会增加女性患乳腺癌和卵巢癌的风险。

Most of these gene mutations are deletions or duplications of one or more exons, and a small amount are point mutations.

基大多数为一个或多个外显子的缺失或重复，小部分是点。

In fact, many different gene mutations have been identified each of which is known to cause different types of spinocerebellar ataxia.

实际上，目前已经鉴定出不同的基；每都会导致不同类型的脊髓小脑性共济失调。

And it's all thanks to a gene mutation.

一切都要归功于基。

Osteosarcoma is linked to RB1 and TP53 genes mutations, while Ewing sarcoma is thought to arise when there are EWSR1, and FLI1 genes mutation.

骨肉瘤与RB1和TP53基有关，尤肉瘤被认为源于EWSR1和FLI1基的易位。

Take a hypothetical gene mutation that proves fatal during childhood.

假设一个在童年时期被证明是致命的基。

Imagine a gene mutation creates a new color of hair.

想像一个新的基异创造出新发色。

Abnormally, an egg could have two naturally occurring gene mutations that don't naturally occur together.

异常情况下，一个鸡蛋可能有两个自然发生的基，但些不会自然发生。

These defects are the result of gene mutations sometimes caused by infectious viruses.

些缺陷是有时由感染性病毒引起的基的结果。

Genetic testing for HEX A gene mutations and sequencing of the HEX A gene are used for diagnosis and heterozygous carrier detection.

HEX-A基检测或HEX-A基测序等可用于诊断该病或发现杂合携带者。

Molecular testing for targetable gene mutations is critical for treatment selection (see Chapter 7).

针对靶向基的分子检测对于治疗选择至关重要（参见第 7 章）。

EGFR mutation EGFR gene mutations were the first driver mutations for which targeted TKI treatments were developed in NSCLC.

EGFR EGFR 基是 NSCLC 中开发靶向 TKI 治疗的第一个驱动。

The results should ease fears that gene mutations alone decide one's brain health, said Rudy Tanzi, a genetics expert at Massachusetts General Hospital.

研究结果应该缓解了人们的担忧，之前大家都担心只有基能决定人类的脑部健康，鲁迪如是说道。