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和基因治疗奠定基础。
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。
Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.
析1组面横裂及附耳家系的临床
现及遗传学特征。
声明:以上例句、词由互联网资源自动生成,部
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。
Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.
析1组面横裂及附耳家系的临床表现及
特征。
声明:以上例句、词性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。
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。
Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.
析1组面横裂
附耳家系的临床表
传学特征。
声明:以上例句、词性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
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变,为进一步开展
诊断和
治疗奠定
础。
Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.
析1组面横裂及附耳家系的临床表现及遗传学特
。
:以上例句、词性
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。
Objective To identify the COL7A1 gene mutation in a family with dy strophic epidermolysis bullosa pruriginosa.
定一痒疹样营养不良型大疱性表皮松解症家系
基因突变,为进一步开展基因诊断和基因治疗奠定基础。
Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.
析1组面横裂及附耳家系
临床表现及遗传学特征。
声明:以上例句、词性类均由互联网资源自动生成,部
人工审核,其表达内容亦不代表本软件
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.
目鉴定一痒疹样营养不良型大疱性表皮松解症家
因突变,为进一步开展
因诊断和
因治疗奠定
础。
Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.
析1组面横裂及附耳家
临床表现及遗传学特征。
声:
例句、词性
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
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。
Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.
析1组面横裂及附耳家系的临床表现及遗传学特征。
声明:以上、词性
类均由互联网资源自动生成,部
未经过人
,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。
Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.
析1组面横裂及附耳家系的临床表现及遗传学特征。
声明:以上例句、词性类均由互联网
动生成,部
未经过人工审核,其表达内容亦
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。
Objective:To observe the clinical symptoms and analyze the hereditary features of a family with hereditary macrostomia and accessory fagus.
析1组面横裂及附耳家系的临床
现及遗传学特征。
声明:以上例句、词互联网资源自动生成,部
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。