Cystic fibrosis is the commonest fatal hereditary disease.
囊性纤维化是最常见的致命性遗传疾病。
这种病遗传吗？
Hereditary hyperekplexia is also called startle disease.
遗传性过度惊骇也被称为惊吓病。
The technique hasn't been approved for use in human reproduction, but could conceivably be used to prevent hereditary, often-fatal mitochondrial disease.
该技术还没有被批准用于人类生殖，但可以设想会用于防止遗传性，这类通常是致命的线粒体疾病。
这是一种家族遗传的疾病吗？
There are no records of a human having been intentionally kept awake long enough to kill them, but a hereditary disease called fatal familial insomnia suggests there is an ultimate limit.
没有关于一个人类被迫保持不睡的时间久到死亡的记录，但是有一种叫做致命性家族失眠症的遗传病似乎表明人类无睡眠时间是有极限的。
Craniomandibular osteopathy is a hereditary disease in West Highland White Terriers and also occurs in other terrier breeds.
前颚骨病是一种常见于西部高地白梗和其他梗类犬的一种遗传病。
It is a recessive hereditary disease of autosome to be deaf and dumb. it was analysed through heredity that reducing or preventing consanguineous marriage can reduce the deaf-mute's birth rate.
聋哑是常染色体隐性遗传病，通过遗传分析发现，减少或防止近亲结婚可以降低聋哑人的出生。
Our babies will be at lower risk for hereditary disease because we are an interracial couple.
我们的孩子患遗传疾病的危险性较低，因为我们是异国情侣。
Family history: family members healthy; denied malignant tumour, heat disease, diabetes, hereditary disease and contagious disease history.
家族史：家庭成员身体健康，否恶性肿瘤、心脏病、糖尿病、遗传病及传染病病史。
The ultimate cause of the disease is unknown, though it is believed to be hereditary.
尽管它具有遗传性，但最根本的病因还未知。
Cordocentesis in this data used in cases with history of hereditary disease, obstetric abnormality, as well as congenital hemolytic infection and blood diseases etc.
本术主要用于宫内诊断遗传疾病，不良孕产史，先天性溶血感染及血液系统疾病等。
AIM To compare the characteristic of the visual electrophysiology between normal SD rats and a case of abnormal rat with retinal hereditary disease.
目的观察正常SD大鼠和一例患遗传性视网膜疾病大鼠的视觉电生理学特点。
Hereditary hearing impairment is caused by genetic defects and is a common clinical disease.
遗传性耳聋由遗传缺陷引起，与基因异常及相关的综合症关系密切，属临床常见疾病。
Congenital fibrosis syndrome is a rare familial hereditary disease, characterized by fibrotic change of extraocular muscles.
先天性纤维化症候群是一少见的家族性遗传疾病。
Oculocutaneous albinism in eye skin is a series of hereditary disease related to melanin biosynthesis, which is mainly short of melanin of eye, skin, hair and brings various hazard to patients.
眼皮肤白化病是一组与黑色素生物合成有关的遗传性疾病，表现为眼、皮肤、毛发黑色素缺乏等。
Sara: That's right. And besides, our babies will be at lower risk for hereditary disease because we're an interracial couple.
莎拉：没错。此外，我们的孩子得遗传疾病的风险会比较低，因为我们是异国情侣。
Objective to analyze the main non hereditary factors influencing plasma homocysteine level in patients with coronary heart disease.
目的分析影响冠心病人血浆同型半胱氨酸水平的主要非遗传因素。
Objective: To investigate the relationship between sterility, spontaneous abortion and abnormal chromosome karyotypes, and that would be help for clinical diagnose for hereditary disease.
目的探讨不孕不育及自发流产与染色体核型异常的关系，指导临床对这些疾病的诊断。
Objective To report a five-generation Chinese family with unidentified maternally transmitted hereditary neurodegenerative disease.
目的报道一个五代母系遗传的未知神经变性疾病家系。
The occurrence of disease is hereditary diseases.
所发生的病就是遗传病。
In this paper, we observed the pathological manifestation of all kinds of disease and made an inquiry into the reason and prevention of hereditary malformation and hyaline membrane disease of newborn.
本文对各种疾病的病理表现进行了观察，并对新生儿肺透明膜病及先天畸形的原因及其预防进行了讨论。
Myotonic muscular dystrophy is a rare hereditary disease involved with multiple sys tems. only a few cases were reported in our country.
强直性肌营养不良症为一种少见的多系统受累的遗传性疾病。
Moreover, it becomes possible to select a respiratory organ such as the lung as a tissue that is capable of producing and supplying a protein deficient in a hereditary disease.
另外，可选择肺等呼吸器官作为供给遗传性疾病所缺失的蛋白质的生产组织。
It also showed concurrence of this disease with other hereditary diseases, such as high myopia and incomplete development of cerebrum, etc.
本病可以与其它遗传病同时发生(如高度近视、大脑发育不全等)，也可以并发其它遗传病(如红绿色盲等)。
The disease has a familial hereditary tendency, genetic research shows a non-singleness genetic character, and the manifestations of its pathogenic gene and mutation site are various.
本病有家族遗传倾向，遗传学研究呈非单一性遗传特点，其致病基因及突变位点表现多样。
The disease has a familial hereditary tendency, genetic research shows a non-singleness genetic character, and the manifestations of its pathogenic gene and mutation site are various.
本病有家族遗传倾向，遗传学研究呈非单一性遗传特点，其致病基因及突变位点表现多样。
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