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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 7201742)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. [Anhidrotic ectodermal dysplasia (Christ-Siemens-Touraine-Syndrome) in an x-linked recessive mode of inheritance (author's transl)].
    Kuhlwein A; Weiss J
    Dermatol Monatsschr; 1982 Jan; 168(1):34-43. PubMed ID: 7200917
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 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. 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]  

  • 10. 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]  

  • 11. Further evidence against linkage between Christ-Siemens-Touraine (CST) and XG loci.
    Chautard-Freire-Maia EA; Primo-Parmo SL; Pinheiro M; Freire-Maia N
    Hum Genet; 1981; 57(2):205-6. PubMed ID: 7194846
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Manifestation of the lines of Blaschko in women heterozygous for X-linked hypohidrotic ectodermal dysplasia.
    Happle R; Frosch PJ
    Clin Genet; 1985 May; 27(5):468-71. PubMed ID: 4006271
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Anhydrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome). A case report.
    Leao JC; Ferreira AM; Bandeira V; Figueirôa FV; Porter SR
    Int Dent J; 2005 Apr; 55(2):89-92. PubMed ID: 15880963
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Hypohidrotic ectodermal dysplasia (Christ-Siemans-Touraine syndrome) in siblings.
    Nathan V
    West Indian Med J; 1984 Mar; 33(1):55-8. PubMed ID: 6730467
    [No Abstract]   [Full Text] [Related]  

  • 18. Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome).
    MacDermot KD; Winter RM; Malcolm S
    Hum Genet; 1986 Oct; 74(2):172-3. PubMed ID: 3464559
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Anhidrotic Ectodermal Dysplasia (Christ-Seimens-Touraine syndrome)--case report with a review.
    Ali G; Kumar M; Verma R; Khajuria V; Wadhwa MB
    Indian J Med Sci; 2000 Dec; 54(12):541-4. PubMed ID: 11354819
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mosaic expression of hypohidrotic ectodermal dysplasia in an isolated affected female child.
    Bartstra HL; Hulsmans RF; Steijlen PM; Ruige M; de Die-Smulders CE; Cassiman JJ
    Arch Dermatol; 1994 Nov; 130(11):1421-4. PubMed ID: 7979445
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.