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因突变,为进一步开展
因诊断和
因治疗奠定
。
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因突变,为进一步开展
因诊断和
因治疗奠定
。
Results Of the 23 mutations, 22 were detected by heteroduplex analysis (96%), 20 by SSCP analysis (87%) and 23 by heteroduplex-SSCP analysis (100%).
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%)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.
目的鉴定痒疹样营养不良型大疱性表皮松解症家系的基因突变,
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
法、SSCP法与异
-SSCP法检出突变分别
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: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
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%)和23
(100%)。
: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.
目的鉴疹样营养不良型大疱性表皮松解症家系的基因突变,为进
步开展基因诊断和基因治疗奠
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,为进一步开展基
诊断和基
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
中ˇ异源双链法、SSCP法与异源双链-SSCP法
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
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
双链法、SSCP法
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,为进一步开展基
诊断和基
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
中ˇ异源双链法、SSCP法与异源双链-SSCP法
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。