Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的突变,为进一步开展
断和
治疗奠定
础。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的突变,为进一步开展
断和
治疗奠定
础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异源
法、SSCP法与异源
-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异
双链法、SSCP法与异
双链-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上、词性分类均由互联网资
生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ
链法、SSCP法与
链-SSCP法检出突变分别为22个(96%)、20个(87%)
23个(100%)。
声明:以上例句、词性分类均由互联网资自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上、词性分类均由互联网资源
成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例句、词性分类均由互联网资源自动生成,部分人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮松解症家系的基因变,为进一步开展基因诊断和基因
定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂
变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出
变分别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱性表皮家系的基因突变,
进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23
杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变分别
22
(96%)、20
(87%)和23
(100%)。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹样营养不良型大疱松解症家系的基因突变,为进一步开展基因诊断
基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23
杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变分别为22
(96%)、20
(87%)
23
(100%)。
明:以上例句、词
分类均由互联网资源自动生成,部分未经过人工审核,其
达内容亦不代
本软件的观点;若发现问题,欢迎向我们指正。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
目的鉴定一痒疹不良型大疱
表皮松解症家系的基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
果23个杂合子突变中ˇ异源双链法、SSCP法与异源双链-SSCP法检出突变
别为22个(96%)、20个(87%)和23个(100%)。
声明:以上例句、词类均由互联网资源自动生成,部
未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。