BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

244 related articles for article (PubMed ID: 3953980)

  • 1. X-linked recessive hypohidrotic ectodermal dysplasia. Manifestations and management.
    Wright JT; Finley WH
    Ala J Med Sci; 1986 Jan; 23(1):84-7. PubMed ID: 3953980
    [No Abstract]   [Full Text] [Related]  

  • 2. [The type of inheritance of anhidrotic ectodermal dysplasia].
    Al'tshuler BA; Suvorova KN
    Vestn Dermatol Venerol; 1984 Feb; (2):15-8. PubMed ID: 6720063
    [No Abstract]   [Full Text] [Related]  

  • 3. [Multiple sebaceous gland hyperplasias in X chromosome hypohidrotic ectodermal dysplasia].
    Orge C; Bonsmann G; Hamm H
    Hautarzt; 1991 Oct; 42(10):645-7. PubMed ID: 1757259
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal recessive hypohidrotic ectodermal dysplasia with subclinical manifestation in the heterozygote.
    Passarge E; Fries E
    Birth Defects Orig Artic Ser; 1977; 13(3C):95-100. PubMed ID: 890117
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Syndromes 17. Hypohidrotic ectodermal dysplasia].
    Baart JA; van Hagen JM
    Ned Tijdschr Tandheelkd; 2000 Jan; 107(1):12-4. PubMed ID: 12621820
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Facial morphometrics in the identification of gene carriers of X-linked hypohidrotic ectodermal dysplasia.
    Saksena SS; Bixler D
    Am J Med Genet; 1990 Jan; 35(1):105-14. PubMed ID: 2301459
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia.
    Zhao J; Hua R; Zhao X; Meng Y; Ao Y; Liu Q; Shang D; Sun M; Lo WH; Zhang X
    Br J Dermatol; 2008 Mar; 158(3):614-7. PubMed ID: 18076698
    [No Abstract]   [Full Text] [Related]  

  • 8. Hypohidrotic ectodermal dysplasia.
    Clarke A
    J Med Genet; 1987 Nov; 24(11):659-63. PubMed ID: 3323518
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia.
    Naeem M; Muhammad D; Ahmad W
    Br J Dermatol; 2005 Jul; 153(1):46-50. PubMed ID: 16029325
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Hypohidrotic (anhidrotic) ectodermal dysplasia in female twins.
    Ogunrinde GO; Zubair RO; Ajike SO; Ige SO
    Niger J Clin Pract; 2012; 15(1):98-100. PubMed ID: 22437101
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features.
    Anton-Lamprecht I; Schleiermacher E; Wolf M
    Birth Defects Orig Artic Ser; 1988; 24(2):183-95. PubMed ID: 3179426
    [No Abstract]   [Full Text] [Related]  

  • 14. Hypohidrotic ectodermal dysplasia--a case report.
    Gopinath VK; Manoj KM; Mahesh K
    J Indian Soc Pedod Prev Dent; 1999 Sep; 17(3):90-2. PubMed ID: 10863497
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Hypodontia and sweat pore counts in detecting carriers of X-linked hypohidrotic ectodermal dysplasia.
    Sofaer JA
    Br Dent J; 1981 Nov; 151(10):327-30. PubMed ID: 6946797
    [No Abstract]   [Full Text] [Related]  

  • 17. Congenital absence of all primary and permanent lateral incisors in a carrier of X-linked hypohidrotic ectodermal dysplasia.
    McLaughlin WS
    Int J Paediatr Dent; 1991 Aug; 1(2):99-103. PubMed ID: 1782201
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications.
    Ferguson BM; Thomas NS; Munoz F; Morgan D; Clarke A; Zonana J
    J Med Genet; 1998 Feb; 35(2):112-5. PubMed ID: 9507389
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hypohidrotic (anhidrotic) ectodermal dysplasia: molecular genetic research and its clinical applications.
    Zonana J
    Semin Dermatol; 1993 Sep; 12(3):241-6. PubMed ID: 8217562
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.