与人类相似的雄性和雌性小鼠不仅性别是不同的，它们各自的遗传反应往往会得到与人们期待相反的药理学结果。
Like their human counterparts, male and female mice are not only different, their respective genetic responses can often be the reverse of what you'd expect from pharmacological results.
PGD适用于特殊遗传病的筛查，如囊性纤维化和神经节苷脂病，而且PGD也可以用于性别选择。
PGD is good for screening for specific genetic disorders such as cystic fibrosis and Tay-Sachs disease, and also can be used to select gender.
遗传，年龄，性别(女性)，怀孕，肥胖和长期站立等影响因素可能会增加静脉曲张的风险。
Factors such as genetics, age, female gender, pregnancy, obesity, and prolonged periods of standing may increase the risk for varicose veins.
可以初步推断，性别、年龄和体重指数可能不是CYP2C19遗传多态性的主要影响因素。
So gender, age and BMI may have no significant effect on genetic polymorphism of CYP2C19.
目的探讨瓣状甲的类型、性别和年龄分布及其遗传方式。
Objective: To research the types, the distributions for gender and age, and the hereditary mode of the petaloid toenails.
其次是为了确定其是否受遗传和性别影响。
The secondary objective was to determine whether the association was modified by familial or genetic effects.
已被广泛熟知的宿主相关因素包括年龄、性别、种族和药物遗传学。
In host related factors, which are generally known as age, gender, race, and pharmacogenetics.
文章主要从生物学角度对人类的遗传性别、性腺性别、体细胞性别和生理性别做了简要的概述。
This paper summarizes the genetic gender, gonad gender, and physiological gender from the biological point of view.
对后代属于罕见性别相关遗传疾病的高危人群的父母来说，这可能是一个好消息，比如男孩的Duchenne肌肉萎缩症和女孩的Turner综合症。
This could be good news for parents whose offspring are at risk of rare gender-related genetic disorders, like Duchenne muscular dystrophy in boys or Turner syndrome in girls.
对后代属于罕见性别相关遗传疾病的高危人群的父母来说，这可能是一个好消息，比如男孩的Duchenne肌肉萎缩症和女孩的Turner综合症。
This could be good news for parents whose offspring are at risk of rare gender-related genetic disorders, like Duchenne muscular dystrophy in boys or Turner syndrome in girls.
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