表皮松解

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

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。

Epidermolysis bullosa is a genetic disorder.

大疱性表皮松解症是一种遗传性疾病。

Causes of Epidermolysis bullosa.

原因大疱性表皮松解症。

Lugalbanda was a god and shepherd king of Uruk where he was worshipped for over a thousand years.

Lugalbanda 是神和被崇拜了一千年多 Uruk古埃及喜克索王朝国王。

I am coming just now,' and went on perfuming himself with Hunut, then he came and sat.

我来只是现在，'歼灭战perfuming自己与胡努特，那麼，他来到和SAT 。