1、

Should We Screen for Familial Intracranial Aneurysm?

我们可筛检家族性颅内动脉瘤 吗 ?

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2、

If a disease has a genetic basis, it will occur in familial aggregates.

如果一种疾病有遗传基础, 它将以家族聚集性的方式发生.

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3、

These are not stories of abusive familial situations, nor of insubordinate young women.

这些不是滥用的家庭情形故事, 也不是关于不听话少妇的故事.

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4、

FvL mutation may be a underlying pathogenicity of familial BCS.

FvL突变可能是家族性BCS的内因.

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5、

Multiple adenomatous polyps of the cecum are seen here in a case of familial polyposis.

图示:家族性肠息肉病的一个病例—盲肠部位的多发性腺瘤性息肉.

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6、

The familial kind are associated with multiple endocrine neoplasia syndrome.

家族发病类型与多发性内分泌瘤综合征有关系.

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7、

In China, the narrative filmic exoterica of familial ethic is one of the most representative types which possess the national idiosyncrasy and embodies the cultural spirit.

在中国,家庭伦理叙事影视作品是最具民族特质,最能彰显民族文化精神的一种影视类型。

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8、

Familial atrophia maculosa varioliformis cutis: Case report and pedigree analysis

皮肤痘疮样斑状萎缩:病例报道及家系调查

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9、

Objective To investigate the relationship between familial aggregation of atopy and asthma phenotypes in children.

目的研究家族特应性聚集与儿童哮喘表型的关系。

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10、

Study on Familial Aggregation in Arteriosclerotic Cerebral Infarction

脑梗塞家族聚集性的研究

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11、

The appearance of afebrile seizures after FS was also independently associated with FS recurrence, and its risk ratio was higher than familial FS history.

FS后出现无热惊厥也与复发性FS独立相关,而且其危险度高于有FS家族史者。

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12、

Objective To map the gene for five Chinese benign familial infantile convulsion ( BFIC) pedigrees.

目的对5个中国良性家族性婴儿惊厥(BFIC)家系进行基因定位研究。

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13、

【 Objectives 】 To research hereditary pattern, clinical features, EEG and chromosomes in one family with benign familial infantile convulsion.

【目的】探讨良性家族性婴儿惊厥(benign familial infantile convulsion,BFIC)一家系的遗传方式、临床特征、脑电图及染色体情况。

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14、

ICCA was defined as consisting of benign familial infantile convulsion ( BFIC) in 3~ 20 months after birth and PKC occurring in later childhood or adolescence.

ICCA的入选标准为:3~20个月出现良性婴儿惊厥(BFIC)和在儿童后期或青春期出现发作性运动源性运动障碍(PKC)。

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15、

Familial goitrous cretinism, report of three cases

家族性甲状腺肿呆小病(克汀病)三例报告

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17、

The paper reports 4 special types of chromaffinoma, including mediastinal, maltiple ectopic malignant, familial and afunctional type, and discusses their diagnoses.

本文报告4例特殊类型的嗜铬细胞瘤,对其诊断问题进行了简要的讨论。

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18、

Background Familial benign chronic pemphigus or Hailey-Hailey disease ( HHD; OMIM 169600) is a rare autosomal dominant cutaneous disorder characterized by recurrent vesicles and erosions mainly in intertriginous areas.

研究背景:家族性慢性良性天疱疮,又称Hailey-Hailey病(HHD,OMIM169600)是一种罕见的常染色体显性遗传性皮肤病。

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19、

Objective To explore the clinical and genetic characteristics of benign familial neonatal convulsion ( BFNC).

目的探讨良性家族性新生儿惊厥(BFNC)的临床特征及遗传学特点。

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20、

Congenital long QT syndrome is a group of familial inherited disease.

先天性Q-T间期延长综合征是一组家族遗传性疾病.

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