159 related articles for article (PubMed ID: 10674821)
1. Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9.
Kono M; Miyamura Y; Matsunaga J; Tomita Y
J Dermatol Sci; 2000 Feb; 22(2):88-95. PubMed ID: 10674821
[TBL] [Abstract][Full Text] [Related]
2. Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21.
Zhang XJ; Gao M; Li M; Li M; Li CR; Cui Y; He PP; Xu SJ; Xiong XY; Wang ZX; Yuan WT; Yang S; Huang W
J Invest Dermatol; 2003 May; 120(5):776-80. PubMed ID: 12713580
[TBL] [Abstract][Full Text] [Related]
3. Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4-cM region at 1q21-22 and a literature review of 136 cases reported in China.
He PP; He CD; Cui Y; Yang S; Xu HH; Li M; Yuan WT; Gao M; Liang YH; Li CR; Xu SJ; Chen JJ; Chen HD; Huang W; Zhang XJ
Br J Dermatol; 2004 Apr; 150(4):633-9. PubMed ID: 15099357
[TBL] [Abstract][Full Text] [Related]
4. A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2.
Xing QH; Wang MT; Chen XD; Feng GY; Ji HY; Yang JD; Gao JJ; Qin W; Qian XQ; Wu SN; He L
Am J Hum Genet; 2003 Aug; 73(2):377-82. PubMed ID: 12815562
[TBL] [Abstract][Full Text] [Related]
5. Dyschromatosis symmetrica hereditaria associated with neurological disorders.
Kondo T; Suzuki T; Ito S; Kono M; Negoro T; Tomita Y
J Dermatol; 2008 Oct; 35(10):662-6. PubMed ID: 19017046
[TBL] [Abstract][Full Text] [Related]
6. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria.
Miyamura Y; Suzuki T; Kono M; Inagaki K; Ito S; Suzuki N; Tomita Y
Am J Hum Genet; 2003 Sep; 73(3):693-9. PubMed ID: 12916015
[TBL] [Abstract][Full Text] [Related]
7. A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.
Li M; Jiang YX; Liu JB; Yang S; He PP; Gao M; Wei SC; Yan KL; Huang W; Zhang XJ
Clin Exp Dermatol; 2004 Sep; 29(5):533-5. PubMed ID: 15347341
[TBL] [Abstract][Full Text] [Related]
8. Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23.
Stuhrmann M; Hennies HC; Bukhari IA; Brakensiek K; Nürnberg G; Becker C; Huebener J; Miranda MC; Frye-Boukhriss H; Knothe S; Schmidtke J; El-Harith EH
Clin Genet; 2008 Jun; 73(6):566-72. PubMed ID: 18462451
[TBL] [Abstract][Full Text] [Related]
9. A new arginine substitution mutation of DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria.
Li CR; Li M; Ma HJ; Luo D; Yang LJ; Wang DG; Zhu XH; Yue XZ; Chen WQ; Zhu WY
J Dermatol Sci; 2005 Feb; 37(2):95-9. PubMed ID: 15659327
[TBL] [Abstract][Full Text] [Related]
10. Hyper- and hypopigmented macules over palms and soles since birth--a case of dyschromatosis symmetrica hereditaria.
Hemmati I; Lam J
Dermatol Online J; 2009 Nov; 15(11):5. PubMed ID: 19951641
[TBL] [Abstract][Full Text] [Related]
11. A novel missense mutation in DSRAD in a family with dyschromatosis symmetrica hereditaria.
Li M; Yang LJ; Shi YX; Huang HY
Arch Dermatol Res; 2007 Aug; 299(5-6):273-5. PubMed ID: 17569068
[TBL] [Abstract][Full Text] [Related]
12. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases.
Oyama M; Shimizu H; Ohata Y; Tajima S; Nishikawa T
Br J Dermatol; 1999 Mar; 140(3):491-6. PubMed ID: 10233273
[TBL] [Abstract][Full Text] [Related]
13. A novel insertion mutation in the ADAR1 gene of a Chinese family with dyschromatosis symmetrica hereditaria.
Zhu CY; Zhu KJ; Zhou Y; Fan YM
Genet Mol Res; 2013 Aug; 12(3):2858-62. PubMed ID: 24065641
[TBL] [Abstract][Full Text] [Related]
14. Identification of a novel mutation in the DSRAD gene in a Chinese pedigree with dyschromatosis symmetrica hereditaria.
Cui Y; Wang J; Yang S; Gao M; Chen JJ; Yan KL; Xiao FL; Huang W; Zhang XJ
Arch Dermatol Res; 2005 May; 296(11):543-5. PubMed ID: 15844011
[TBL] [Abstract][Full Text] [Related]
15. Seven novel mutations of ADAR in multi-ethnic pedigrees with dyschromatosis symmetrica hereditaria in China.
Wang P; Yu S; Liu J; Zhang D; Kang X
Mol Genet Genomic Med; 2019 Oct; 7(10):e00905. PubMed ID: 31423758
[TBL] [Abstract][Full Text] [Related]
16. Dyschromatosis symmetrica hereditaria.
Hayashi M; Suzuki T
J Dermatol; 2013 May; 40(5):336-43. PubMed ID: 22974014
[TBL] [Abstract][Full Text] [Related]
17. Identification of two novel mutations in Chinese patients with Dyschromatosis symmetrica hereditaria.
Li M; Li C; Hua H; Zhu W; Lu Y; Yang L
Arch Dermatol Res; 2005 Nov; 297(5):196-200. PubMed ID: 16215765
[TBL] [Abstract][Full Text] [Related]
18. Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report.
Patrizi A; Manneschi V; Pini A; Baioni E; Ghetti P
Acta Derm Venereol; 1994 Mar; 74(2):135-7. PubMed ID: 7911621
[TBL] [Abstract][Full Text] [Related]
19. A new mutation of the double-stranded RNA-specific adenosine deaminase gene in a family with dyschromatosis symmetrica hereditaria.
Liu Y; Xiao S; Peng Z; Chu Y; Wang J; Li X; Zhou S
Dermatology; 2006; 213(3):200-3. PubMed ID: 17033168
[TBL] [Abstract][Full Text] [Related]
20. Identification of a novel DSRAD gene mutation in a Chinese family with dyschromatosis symmetrica hereditaria.
Li M; Yang LJ; Zhu XH
Clin Exp Dermatol; 2008 Aug; 33(5):644-6. PubMed ID: 18627385
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
