These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
156 related articles for article (PubMed ID: 2912882)
1. Hypohidrotic ectodermal dysplasia. Clinical study of a family of 30 over three generations. Gilgenkrantz S; Blanchet-Bardon C; Nazzaro V; Formiga L; Mujica P; Alembik Y Hum Genet; 1989 Jan; 81(2):120-2. PubMed ID: 2912882 [TBL] [Abstract][Full Text] [Related]
2. Carrier detection in Christ-Siemens-Touraine syndrome (X-linked hypohidrotic ectodermal dysplasia). Freire-Maia N; Pinheiro M Am J Hum Genet; 1982 Jul; 34(4):672-4. PubMed ID: 7201742 [No Abstract] [Full Text] [Related]
3. Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis. Zonana J; Sarfarazi M; Thomas NS; Clarke A; Marymee K; Harper PS J Pediatr; 1989 Mar; 114(3):392-9. PubMed ID: 2564048 [TBL] [Abstract][Full Text] [Related]
4. X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis. Zonana J; Clarke A; Sarfarazi M; Thomas NS; Roberts K; Marymee K; Harper PS Am J Hum Genet; 1988 Jul; 43(1):75-85. PubMed ID: 3163892 [TBL] [Abstract][Full Text] [Related]
5. Hypohidrotic ectodermal dysplasia: argument against an autosomal recessive form clinically indistinguishable from X-linked hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome). Sybert VP Pediatr Dermatol; 1989 Jun; 6(2):76-81. PubMed ID: 2748478 [TBL] [Abstract][Full Text] [Related]
6. Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasia. Goodship J; Malcolm S; Clarke A; Pembrey ME J Med Genet; 1990 Jul; 27(7):422-5. PubMed ID: 2395159 [TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis. Zonana J; Schinzel A; Upadhyaya M; Thomas NS; Anton-Lamprecht I; Harper PS Am J Med Genet; 1990 Jan; 35(1):132-5. PubMed ID: 2301463 [TBL] [Abstract][Full Text] [Related]
8. A novel missense mutation (402C-->T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasia. Hertz JM; Nørgaard Hansen K; Juncker I; Kjeldsen M; Gregersen N Clin Genet; 1998 Mar; 53(3):205-9. PubMed ID: 9630076 [TBL] [Abstract][Full Text] [Related]
9. Christ-Siemens-Touraine syndrome. Investigations on two large Brazilian kindreds with a new estimate of the manifestation rate among carriers. Pinheiro M; Ideriha MT; Chautard-Freire-Maia EA; Freire-Maia N; Primo-Parmo SL Hum Genet; 1981; 57(4):428-31. PubMed ID: 7286985 [No Abstract] [Full Text] [Related]
11. Pitfalls in clinical diagnosis of female carriers of X-linked hypohidrotic ectodermal dysplasia. Vincent MC; Cossée M; Vabres P; Stewart F; Bonneau D; Calvas P Arch Dermatol; 2002 Sep; 138(9):1256-8. PubMed ID: 12225002 [No Abstract] [Full Text] [Related]
12. A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia. Nakata M; Koshiba H; Eto K; Nance WE Am J Hum Genet; 1980 Nov; 32(6):908-19. PubMed ID: 7446529 [TBL] [Abstract][Full Text] [Related]
13. Scaling skin in the neonate: a clue to the early diagnosis of X-linked hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome). The Executive and Scientific Advisory Boards of the National Foundation for Ectodermal Dysplasias, Mascoutah, Illinois. J Pediatr; 1989 Apr; 114(4 Pt 1):600-2. PubMed ID: 2926570 [No Abstract] [Full Text] [Related]
14. Mutation analysis of X-linked hypohidrotic ectodermal dysplasia in a Taiwanese family. Chao SC; Chung CH; Yang CC; Yang MH; Lee JY J Formos Med Assoc; 2003 Jun; 102(6):412-7. PubMed ID: 12923595 [TBL] [Abstract][Full Text] [Related]
16. A novel 7-bp deletion mutation in a Taiwanese family with X-linked hypohidrotic ectodermal dysplasia. Lin TK; Huang CY; Lin MH; Chao SC Clin Exp Dermatol; 2004 Sep; 29(5):536-8. PubMed ID: 15347342 [TBL] [Abstract][Full Text] [Related]
17. Christ-Siemens-Touraine syndrome--a clinical and genetic analysis of a large Brazilian kindred: III. Carrier detection. Pinheiro M; Freire-Maia N Am J Med Genet; 1979; 4(2):129-34. PubMed ID: 517572 [TBL] [Abstract][Full Text] [Related]
18. Molecular genetic analysis of consanguineous Pakistani families with autosomal recessive hypohidrotic ectodermal dysplasia. Bibi N; Ahmad S; Ahmad W; Naeem M Australas J Dermatol; 2011 Feb; 52(1):37-42. PubMed ID: 21332691 [TBL] [Abstract][Full Text] [Related]
19. A dental approach to carrier screening in X linked hypohidrotic ectodermal dysplasia. Spfaer JA J Med Genet; 1981 Dec; 18(6):459-60. PubMed ID: 7334506 [TBL] [Abstract][Full Text] [Related]
20. Anhidrosis and absence of sweat glands in mice hemizygous for the Tabby gene: supportive evidence for the hypothesis of homology between Tabby and human anhidrotic (hypohidrotic) ectodermal dysplasia (Christ-Siemens-Touraine syndrome). Blecher SR J Invest Dermatol; 1986 Dec; 87(6):720-2. PubMed ID: 3782855 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]