英语人>网络例句>epidermolysis 相关的网络例句
epidermolysis相关的网络例句

查询词典 epidermolysis

与 epidermolysis 相关的网络例句 [注:此内容来源于网络,仅供参考]

The mutation of G2034R is the underlying cause of epidermolysis bullosa pruriginosa in this family, not common polymorphism.

G2034R突变是引起该家系临床病变的特异突变,不是多态性变化。

Epidermolysis bullosa is normally diagnosed on a combination of the clinical symptoms and family history, with a skin tissue sample and mutation analysis.

大疱性表皮松解症通常是诊断上的结合临床症状及家族病史,与皮肤组织样本和突变分析。

Objective To evaluate the significance of mouse anti-human monoclonal antibody LH 7∶2 in the diagnosis of distrophic epidermolysis bullosa.

目的 探讨鼠抗人单克隆抗体LH 7∶2诊断营养不良型大疱性表皮松解症的意义。

To Leshan to see the two "hereditary epidermolysis bullosa" children.

4月23日,到乐山看望两个"遗传性大疱性表皮松解症"的孩子。

To identify additional epidermolysis bullosa simplex mutations for studying the correlation between genotype and phenotype of EBS, and to provide basis for genetic counselling, as well as for gene diagnosis and gene therapy..

目的鉴定更多的单纯型大疱性表皮松解症突变以研究EBS基因型和表型关系,为EBS的遗传咨询及基因诊断和基因治疗奠定基础。

Objective To identify additional epidermolysis bullosa simplex mutations for studying the correlation between genotype and phenotype of EBS, and to provide basis for genetic counselling, as well as for gene diagnosis and gene therapy..

目的鉴定更多的单纯型大疱性表皮松解症突变以研究EBS基因型和表型关系,为EBS的遗传咨询及基因诊断和基因治疗奠定基础。

Mouse anti-human monoclonal antibody LH7∶2 is helpful to improve diagnosis of distrophic epidermolysis bullosa.

鼠抗人单克隆抗体LH 7∶2诊断营养不良性大疱性表皮松解症有重要意义

Jordan Young is one of only five children in Britain with epidermolysis bullosa, a painful condition that means his skin suffers irritation every time it comes in contact with ordinary materials.

英国一名只有1岁大的小童由于罹患可致命的罕见皮肤失调的怪病,只能接触真丝和绸缎,就连尿片也必须以丝绸缝制。

Epidermolysis bullosa represents a group of genodermatoses characterized by fragility, easy blistering of the skin and mucous membranes.

遗传性大疱型表皮松解症是一组皮肤、粘膜脆性增加,容易出现水疱大疱的遗传性皮肤病。

Background: Epidermolysis bullosa is a rare disease that is usually inherited, begins early in life, and results in bullae and erosion at sites of trauma, usually on the hands, elbows, knees, and feet.

背景: 大疱性表皮松解症是一种罕疾病,通常有遗传性、生命的早期发病、导致受伤部位有大水疱与糜腐蚀形成,通常发生在手、手肘、膝盖和脚。

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