Six novel mutations of ADAR1 gene with dyschromatosis symmetrica hereditaria;
遗传性对称性色素异常症6个新的致病基因突变研究
Detection of mutation of DSRAD of a patient with atypical vitiligo in a family of dyschromatosis symmetrica hereditaria;
遗传性对称性色素异常症一家系中不典型白癜风患者1例
Background Dyschromatosis symmetrica hereditaria (DSH, 0MIM#127400) is an autosomal dominant pigmentary genodermatosis characterized by hyperpigmented and hypopigmented macules of on the extremities.
遗传性对称性色素异常症(DGH，OMIM#127400)是一种以肢端对称分布色素沉着和色素减退斑为特怔的常染色体显性遗传病，婴儿期或儿童期发病，在亚洲人中较常见。
Study on Clinical Character and Genetic Model of Dyschromatosis Symmetrical Hereditaria and Freckle;
遗传性对称性色素异常症和雀斑的临床特点和遗传方式研究
One case of dyschromatosis universalis hereditaria;
遗传性泛发性色素异常症1例
Identification of Novel Mutations in the ADAR Gene of Dyschromatosis Symmetrica Hereditaria (DSH)
遗传性对称性色素异常症基因新突变的发现
Study on the Mutations of ADAR1 Gene in the Patients with Dyschromatosis Symmetrica Hereditaria;
遗传性对称性色素异常症致病基因突变研究
Mutation of Two Families with Dyschromatosis Symmetrical Hereditaria
遗传性对称性色素异常症家系的DSRAD基因突变
Study on Clinical Character and Genetic Model of Dyschromatosis Symmetrical Hereditaria and Freckle;
遗传性对称性色素异常症和雀斑的临床特点和遗传方式研究
Mutation Identification and Functional Analysis of ADAR, the Disease Gene for Dyschromatosis Symmetrica Hereditaria
遗传性对称性色素异常症致病基因的突变鉴定和功能分析
Localization of DSH-associated Gene and Identification of the Gene Mutation;
遗传性对称性色素异常症致病基因的定位和突变研究
Identification of a Locus for Dyschromatosis Symmetrica Hereditaria by Genome-wide Scan;
全基因组扫描定位遗传性对称性色素异常症易感区域
A nonsense mutation of ADAR gene in a sporadic patient with dyschromatosis symmetrica hereditaria
1例遗传性对称性色素异常症患者ADAR基因突变研究
Two Novel Mutation of the DSRAD Gene with Dyschromatosis Symmetrica Hereditary
遗传性对称性色素异常症2个新的致病基因突变检测
A Novel Mutation of ADAR Gene Identified in a Chinese Pedigree with Dyschromatosis Symmetrical Hereditaria
遗传性对称性色素异常症一家系中ADAR基因的新突变
hereditary enamel dysplasia
遗传性釉质发育异常症
MATERNALLY INHERITED "SONLESS" ABNORMAL SEX-RATIO CONDITION IN THE LADY-BEETLE (HARMONIA AXYRIDIS)
异色瓢虫“单生雌”性比异常的母系遗传
hereditary hyperbilirubinemia
遗传性高胆血红素症
sex-limited autosomal dominant inheritance
性限常染色体显性遗传;限性常染色体显性遗传
an inherited form of anemia caused by faulty synthesis of hemoglobin.
由于血色素合成有误引起的遗传性贫血症。
Genetic Diversity of Silurus asotus on Mitochondrial Cytochrome b Gene Sequence
鲇细胞色素b基因序列差异及遗传多样性分析
HHT is an autosomal dominant disordercharacterized by vascular dysplasia.
HHT是常染色体显性遗传性血管发育异常的一种疾病。
This is tuberous sclerosis, an autosomal dominant condition characterized by mental retardation and seizures beginning early in life.
结节性硬化症，常染色体显性遗传，表现为智力低下、癫痫发作等。