1)Marie Unna Hereditary HypotrichosisMarie Unna型遗传性稀毛症
1.Mutation Analysis and Functional Study of U2HR in Chinese Patients with Marie Unna Hereditary HypotrichosisMarie Unna型遗传性稀毛症致病基因突变筛查及功能研究
英文短句/例句
1.Mutation Analysis and Functional Study of U2HR in Chinese Patients with Marie Unna Hereditary HypotrichosisMarie Unna型遗传性稀毛症致病基因突变筛查及功能研究
2.Gene Mutations in Psoriasis and Marie Unna Hereditary Hypotrichosis银屑病及Marie Unna遗传性稀毛症的遗传易感基因
3.Advance in Clinical and Molecular Genetics Study of Charcot-Marie-Tooth Disease 1X Type (review)Charcot-Marie-Tooth病1X型的临床与分子遗传学研究进展
4.hereditary hemorrhagic telangiectasia遗传性出血性毛细血管扩张症
5.Gene Mapping of a Hereditary Hypotrichosis Simplex Family;一遗传性单纯少毛症家系的基因定位
6.Mutation Analysis of ALK1 Gene in a Chinese Family with Hereditary Hemorrhagic Telangiectasis Type Ⅱ;遗传性出血性毛细血管扩张症ALK1基因突变研究
7.Determination of Mutations in ALK-1 Gene in Chinese Family with Hereditary Hemorrhagic Telangiectasia Disease;一个遗传性出血性毛细血管扩张症家系ALK-1基因突变检测
8.Examination techniques and imaging findings in patients with hereditary hemorrhagic telangiectasia遗传性出血性毛细血管扩张症的检查方法和影像学表现
9.Color Doppler ultrasound in diagnosis of hereditary hemorrhagic telangiectasia with hepatic involvement彩超诊断累及肝脏的遗传性出血性毛细血管扩张症
10.A case of recessive dystrophic epidermolysis bullosa隐性遗传营养不良型大疱性表皮松解症1例
11.Congenital Generalized Hypertrichosis Terminalis: Genetic Mapping and Pathogenic Mutation Identification先天性全身终毛增多症的遗传学定位和致病突变研究
12.The Genetic Diversity of Dendrolimus Tabulaeformis in Forests of Different Stand Types;不同林分类型油松毛虫种群遗传多样性研究
13.Microsatellate Analysis of Genetic Diversity and Wool Traits in Superfine Merino Sheep;超细型细毛羊遗传多样性及羊毛性状的微卫星分析
14.hereditary hyperbilirubinemia遗传性高胆血红素症
15.genetic goitrous cretinism遗传性甲状腺呆小症
16.hereditary enamel dysplasia遗传性釉质发育异常症
17.Analysis of Genetic Diversity of American Rex and Su-line Angora Rabbit美系獭兔和苏Ⅰ系粗毛型长毛兔的遗传多样性分析
18.Phenotype and genotype diagnosis in five Chinese pedigrees with Glanzmann thrombasthenia五个遗传性血小板无力症家系的表型和基因型诊断
相关短句/例句
Marie Unna hereditary hypotrichosis (MUHH)Marie Unna遗传性稀毛症(MUHH)
3)Charcot-Marie-Tooth disease 1X typeCharcot-Marie-Tooth病1X型
4)Charcot-Marie-Tooth DiseaseCharcot-Marie-Tooth病
5)Marie's methodMarie方法
6)Charcot-Marie-Tooth disease(CMT)Charcot-Marie-Tooth病(CMT)
1.Objective To analyse the characteristics of symptoms,signs and electrophysiology in Charcot-Marie-Tooth disease(CMT)with peripheral myelin protein 22(PMP22)gene duplication abnormality.目的分析Charcot-Marie-Tooth病(CMT)周围髓鞘蛋白22(PMP22)基因重复异常患者临床症状、体征和电生理特点。
延伸阅读
[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]分子式：C16H16ClN3O3S分子量：365.5CAS号：26807-65-8性质：暂无制备方法：暂无用途：用于轻、中度原发性高血压。
