1.
A case of reticulate pigmented anomaly of the flexures is reported.
【中英文摘要】报告1例皱褶部网状色素异常症。
2.
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
3.
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
4.
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
5.
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
6.
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
7.
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
8.
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
9.
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
10.
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
11.
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
12.
Chromosomal disorder: Syndrome caused by chromosome abnormality.
染色体疾病:因染色体的异常导致的症候。
13.
Insulin resistance and abnormal function of vascular endothelium cell: is high blood free fatty acid play a key role?
胰岛素抵抗与血管内皮细胞功能异常--高游离脂肪酸血症扮演了主要角色?
14.
Unusual red pigmentation, as of hair or plumage.
异常的红色素沉着异常的红色素沉着，像红须发或红羽毛
15.
Chromosomal karyotype analysis in 69 patients with myelodysplastic syndrome
69例骨髓增生异常综合症染色体核型分析
16.
a condition characterized by abnormal deposits of melanin (especially in the skin).
黑色素在皮肤上的异常堆积。
17.
hereditary enamel dysplasia
遗传性釉质发育异常症
18.
abnormal patency of eustachian tube
咽鼓管异常开放(症)