Study on the Causes of Anormalous Water Level Changes in Huoshan 33 Well,Anhui Province
霍山皖33井水位突变异常成因的研究
To mutate or change morphologically, often reversibly.
突变，变异经受突变或形态上的改变，常为可逆地
Changes of α-synuclein After Accumulation
α-突触核蛋白异常沉积后的成分改变
The Mutations and Protein Expressions of PTEN and p53 Genes in Malignant Transformation of Endometriosis
PTEN和p53基因突变和蛋白异常表达与子宫内膜异位症恶变的关系
Müllerian anomalies,hearing loss,and connexin 26 mutations
苗勒管发育异常、听力丧失与连接蛋白26突变
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
Study of Mutations on the D-Loop Region of Mitochondrial DNA in Myelodysplastic Syndrome;
骨髓增生异常综合征线粒体DNA D-loop区突变研究
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
Most of an individual's genes, however, are inherently good.
然而人类个体的基因生来就是正常的，很少发生突变（变异）。
Even in these days of rapid technological change, the abruptness of this transition was unusual.
即使在目前技术日新月异的时代，这个转变的突然性也是不寻常的。
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
Its gravitational field is on a density suddenchange belt of Bouguer anomaly isopleth.
重力场则处于布伽重力异常等值线疏密突变带上。
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
Mutations in the D-LOOP Region of Mitochondrial DNA in Myelodysplastic Syndrome;
骨髓增生异常综合征线粒体DNA D-LOOP区突变的研究
Study on Mitochondria Cytochrome Oxidase (CO Ⅰ.Ⅱ) Gene Mutation in Patients with Myelodysplastic Syndromes;
骨髓增生异常综合征与线粒体细胞色素氧化酶基因突变
Study on STK15 Gene Overexpression and p53 Gene Mutation in Centrosomal Abnormality of Laryngeal Carcinoma;
喉癌p53基因突变和STK15基因过表达与中心体异常相关性研究
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
