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

这种适应包括改企鹅看方式基因。

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

最后，可以通过基因检测寻找异常血红蛋白基因进行确诊。

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

也可对已知与Kallmann综合征相关基因进行基因检测。

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

此外，还可以预见新基因治疗手段通过纠正特定来治疗疾病。

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

“根据对白熊和棕熊研究，这可能是基因。

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

存在HMBS基因及缺乏卟原脱氨酶人群大部分没有症状。

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

对她案件调查发现，她孩子们可能是因为极其罕见基因，属于自然死亡。

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

她BRCA1和BRCA2基因检测呈阴性，而这种基因会增加女性患乳腺癌和卵巢癌风险。

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

基因大多数为一个或多个外显子缺失或重复，小部分是点。

10.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基因；每种都会导致不同类型脊髓小脑性共济失调。

11.And it's all thanks to a gene mutation.

而这一切都要归功于基因。机翻

12.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基因有关，尤因肉瘤被认为源于EWSR1和FLI1基因易位。

13.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基因。机翻

14.Imagine a gene mutation creates a new color of hair.

想像一个新基因异创造出新发色。

15.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基因，但这些不会自然发生。机翻

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

这些缺陷是有时由感染性病毒引起基因结果。

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

HEX-A基因检测或HEX-A基因测序等可用于诊断该病或发现杂合携带者。

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

针对靶向基因分子检测对于治疗选择至关重要（参见第 7 章）。机翻

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

EGFR EGFR 基因是 NSCLC 中开发靶向 TKI 治疗第一个驱动。机翻

20.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担忧，之前大家都担心只有基因能决定人类脑部健康，鲁迪如是说道。