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。
Primary liver cancer was seen as a hereditary disease of multiple genes, and also-was a product which were caused by combination of many factors.
原发性肝癌被视为多基因遗传病，同时，又是多种因素共同作用的产物。
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。
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。
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。
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。
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。
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。
Cancer is a disease with disorder of cell cycle and uncontrolled growth due to the common effects of hereditary factor and environmental factor.
肿瘤是遗传因素和环境因素共同作用下细胞周期紊乱、细胞失控性生长所致的一类疾病。
Orthodox study mode on multiple factor disease and large sample perspective study indicate that hereditary factor is a considerable role in the process of alcohol dependence pathogenesis.
传统的多因子疾病研究方法以及大样本前瞻性研究表明遗传因素在酒依赖发病过程中起重要作用。
This gene transfer into airway epithelial stem cells with the use of the vector as described above is useful in gene therapy for a hereditary respiratory disease such as cystic fibrosis.
使用本发明的载体将基因导入到呼吸道上皮组织干细胞可基因治疗囊性纤维症等遗传性呼吸系统疾病。
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。
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 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。
Hereditary disease is a kind of disease that is greatly harmful to human health. It affects severely population quality.
遗传病是对人类健康危害极大的一种疾病，它严重影响人口素质。
At Cornell University, researchers are pursuing gene-based therapies for Parkinson's disease and a rare hereditary disorder that destroys children's brain cells.
在康奈尔大学，研究人员正在研究用基因疗法治疗帕金森症和一种破坏儿童脑细胞的罕见遗传疾病。
This is the indirect and genetic pattern of a kind of cancer, namely this kind of hereditary disease is in in the future 50% become cancer, say cancer is OK so genetic.
这是一种癌症的间接遗传方式，即这种遗传病在将来50%成为癌症，所以说癌症是可以遗传的。
Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease (ROW) is a disorder that presents with recurrent episodes of EPX.
遗传性毛细血管扩张症(HHT)或Rendu - Osler - Weberdisease (ROW)是一种表现为反复出血发作的障碍。
Hereditary hemorrhagic telangiectasia is an uncommon autosomal dominant inheritance disease. 25 cases from a family were reported. The pathology, clinical presentation and treatment were discussed.
遗传出血性毛细血管扩张症为常染色体显性遗传病，临床少见，本文就其病理变化、临床特点进行讨论，探讨其治疗方法。附一家系25例分析。
Whether to have a kind of hereditary disease: "Omnibus complication" a kind of what kind of disease is it?
是否有一种遗传病：“综合性并发症”它是一种什么样的病呢？
WD is a drug-treatable hereditary disease, which is rare. However without reasonable treatment, outcome is often fatal.
WD是少有的可用药物治疗的遗传病，但未经合理的治疗后果往往是致命性的。
WD is a drug-treatable hereditary disease, which is rare. However without reasonable treatment, outcome is often fatal.
WD是少有的可用药物治疗的遗传病，但未经合理的治疗后果往往是致命性的。
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