BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 7334506)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Clinical and radiographic dental findings in X linked hypohidrotic ectodermal dysplasia.
    Crawford PJ; Aldred MJ; Clarke A
    J Med Genet; 1991 Mar; 28(3):181-5. PubMed ID: 2051453
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Primary anodontia in X-linked hidrotic ectodermal dysplasia].
    Beliakov IuA; Elizarova VM; Smirnova TA; Krotov VA
    Stomatologiia (Mosk); 1998; 77(4):29-31. PubMed ID: 9752735
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Sweat testing to identify female carriers of X linked hypohidrotic ectodermal dysplasia.
    Clarke A; Burn J
    J Med Genet; 1991 May; 28(5):330-3. PubMed ID: 1865470
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Clinical aspects of X-linked hypohidrotic ectodermal dysplasia.
    Clarke A; Phillips DI; Brown R; Harper PS
    Arch Dis Child; 1987 Oct; 62(10):989-96. PubMed ID: 2445301
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Anhidrotic ectodermal dysplasia (apropos of 3 families). Abnormal hair, a sign of heterozygosity?].
    Le Marec B; Roussey M; Chevrant-Breton J; Segalen J; Bourdinière J; Sénécal J
    J Genet Hum; 1983 Dec; 31(4):279-93. PubMed ID: 6663288
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hypohidrotic ectodermal dysplasia: dental features and carriers detection.
    Glavina D; Majstorović M; Lulić-Dukić O; Jurić H
    Coll Antropol; 2001 Jun; 25(1):303-10. PubMed ID: 11787554
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Familial ectodermal dysplasia: a peers' agony.
    Hegde K; Kashyap RR; Nair G; Nair PP
    BMJ Case Rep; 2013 Jul; 2013():. PubMed ID: 23880572
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Hypohidrotic and hidrotic ectodermal dysplasia: a report of two cases.
    Vasconcelos Carvalho M; Romero Souto de Sousa J; Paiva Correa de Melo F; Fonseca Faro T; Nunes Santos AC; Carvalho S; Veras Sobral AP
    Dermatol Online J; 2013 Jul; 19(7):18985. PubMed ID: 24010518
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expression of X-linked hypohidrotic ectodermal dysplasia in six males and in their mothers.
    Söderholm AL; Kaitila I
    Clin Genet; 1985 Aug; 28(2):136-44. PubMed ID: 4042395
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A clinico-pathologic presentation. Hereditary hypohidrotic ectodermal dysplasia, or HED.
    Cataldo E; Santis HR
    J Mass Dent Soc; 1996; 45(1):8. PubMed ID: 9520670
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.