• 也是一种遗传畸形

    It is also a genetic freak.

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  • 兄妹之间通婚缺陷基因两份拷贝都传递给下一代,他们所生育的后代容易产生各种遗传缺陷例如图坦卡蒙畸形

    Married siblings are more likely to pass on twin copies of harmful genes, leaving their children vulnerable to a variety of genetic defects. Tutankhamun's malformed foot may have been one such flaw.

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  • 科学家可能已经取得状贫血病治疗技术项重大进步。镰状贫血病是一种造成血细胞畸形常见遗传

    Scientists have taken a potentially important step toward a therapy for sickle cell disease, a common genetic disorder characterized by malformed red blood cells.

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  • 这只名叫弗兰克的猫它的主人米巴里美国马萨诸塞州遗传面部畸形,使长出额外的一张脸。

    Frankenlouie, who lives with his owner in Milbury, Massachusetts, has a genetic birth deformity which caused him to grow the extra facial features.

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  • 尽管ART孩子先天畸形普通孩子一点点,但是他们遗传紊乱病,例如贝威氏综合症风险要搞4.56

    Although ART children had a slightly higher than normal rate of birth defects, their risk of developing epigenetic disorders, such as Beckwith-Wiedemann syndrome, was 4.5 to six times higher.

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  • 结论先天畸形遗传早期环境因素直接关系

    Conclution the congenital malformation have direct relation with the heredity and the environment in the pregnancy.

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  • 结论先天畸形遗传因素早期环境因素直接关系

    Conclusion: the congenital malformation have direct relation with the genetic factor and environmental factor in early pregnancy.

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  • 畸形新生儿有时重组以及儿童感染性遗传疾病相关

    Birth defects can also be associated with rearrangements, and genetic disease among affected children.

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  • 遗传疾病先天性畸形变形染色体异常

    The insured suffers from inherited disease, congenital abnormality, deformation or chromosome abnormality.

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  • 结果遗传、家族史病例,其胎儿畸形发病率明显增高

    Result The occurrence of fetal abnormalities was much more higher in the group with family history and inheritance history.

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  • 均无耳聋病史其它部位畸形结论:杯状耳形成父母双方中方杯状耳基因决定的,系分析显示为常染色体显性遗传

    Conclusion:The family investigation suggested that the formation of cup ear was determined by the cup ear gene of an affected parent and it was an autosomal dominant inheritance.

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  • 目的探讨髂骨骨尺骨延长治疗遗传多发性骨软骨瘤所致前臂畸形的疗效

    Objective: To discuss the effect of ilium grafting and ulna lengthening on the treatment of forearm deformity of heredity multiple osteochondroma.

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  • 目的调查海南黎族0 ~14儿童遗传先天性畸形分布患病率

    Objective: To investigate the distribution and morbidity of inherited disease and congenital deformity of0 ~ 14years old children of li nationality in Hainan island.

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  • 畸形基因遗传病,表现家族遗传倾向

    Wrong tooth adds up to deformation is polygene hereditary disease, often behave familial and genetic tendency.

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  • 糖尿病合并妊娠引起胎儿心脏畸形先天性心脏病重要遗传风险因素

    Pregestational diabetes mellitus may cause fetal heart defects, and it is considered to be an important non-genetic risk factors for congenital heart defects.

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  • 采用乳牛外周血淋巴细胞作短期培养空气干燥法制备染色体。对临床诊断为输卵管阻塞1生殖器官畸形5进行细胞遗传分析

    Comparetive chromosome studies wore carried out by means of short culture of lymphocytes from peripheral blood of 1 cow with simple salpingo obstruction and 5 cows with reproduction system problems.

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  • 以上的自然流产是因为胎儿遗传缺陷可能会造成致命畸形

    More than 60% are caused by an inherited defect in the fetus, which might result in a fatal abnormality.

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  • 方法利用表达序列标签克隆策略选择了1个可能遗传骨性反颌畸形相关候选基因——OT X1。

    Methods a candidate gene associated with hereditary bone crossbite deformity-OTX1 was chosen by expressed sequence tags cloning strategy.

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  • 虽然遗传变异会导致一些畸形,但是,许多人包括双面畸形发育期间面临障碍引起的。

    While genetic mutations cause some abnormalities in humans , many , including diprosopia , are caused by obstacles faced during development .

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  • 科学家可能已经取得状贫血病治疗技术项重大进步。镰状贫血病是一种造成血细胞畸形常见遗传病。

    Scientists have taken a potentially important step toward a therapy for sickle cell disease a common genetic disorder characterized by malformed red blood cells.

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  • 近亲婚配家族各种遗传先天畸形发病率明显高于非近亲婚配家族。

    The morbidity of various inherited diseases and congenital monstrosity infants in near relative wedding sept was clearly higher than that in non-near relative wedding sept. ?CONCLU SION?

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  • 综合征一种X连锁隐性遗传病,为男性假两性畸形常见类型

    Testicular feminization syndrome, the most common type of male pseudohermaphroditism, is an X-linked recessive disorder.

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  • 综合征一种X连锁隐性遗传病,为男性假两性畸形常见类型

    Testicular feminization syndrome, the most common type of male pseudohermaphroditism, is an X-linked recessive disorder.

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