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 *

206 related articles for article (PubMed ID: 10677098)

  • 1. Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia.
    Cambiaghi S; Restano L; Pääkkönen K; Caputo R; Kere J
    Arch Dermatol; 2000 Feb; 136(2):217-24. PubMed ID: 10677098
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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. Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder.
    Munoz F; Lestringant G; Sybert V; Frydman M; Alswaini A; Frossard PM; Jorgenson R; Zonana J
    Am J Hum Genet; 1997 Jul; 61(1):94-100. PubMed ID: 9245989
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia.
    van der Hout AH; Oudesluijs GG; Venema A; Verheij JB; Mol BG; Rump P; Brunner HG; Vos YJ; van Essen AJ
    Eur J Hum Genet; 2008 Jun; 16(6):673-9. PubMed ID: 18231121
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Prenatal Genetic Testing for X-Linked Hypohidrotic Ectodermal Dysplasia.
    Yapijakis C; Gintoni I; Chrousos G
    Adv Exp Med Biol; 2021; 1339():337-340. PubMed ID: 35023123
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO).
    Zonana J; Elder ME; Schneider LC; Orlow SJ; Moss C; Golabi M; Shapira SK; Farndon PA; Wara DW; Emmal SA; Ferguson BM
    Am J Hum Genet; 2000 Dec; 67(6):1555-62. PubMed ID: 11047757
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Clinical and Molecular Genetic Analysis of Cases with Ectodermal Dysplasia.
    Yapijakis C; Douka A; Gintoni I; Agiannitopoulos K; Vlachakis D; Chrousos GP
    Adv Exp Med Biol; 2023; 1423():181-186. PubMed ID: 37525042
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A rare case of hypohidrotic ectodermal dysplasia caused by compound heterozygous mutations in the EDAR gene.
    Shimomura Y; Sato N; Miyashita A; Hashimoto T; Ito M; Kuwano R
    J Invest Dermatol; 2004 Oct; 123(4):649-55. PubMed ID: 15373768
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Α de novo 3.8-Mb inversion affecting the EDA and XIST genes in a heterozygous female calf with generalized hypohidrotic ectodermal dysplasia.
    Escouflaire C; Rebours E; Charles M; Orellana S; Cano M; Rivière J; Grohs C; Hayes H; Capitan A
    BMC Genomics; 2019 Sep; 20(1):715. PubMed ID: 31533624
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Orofacial features of hypohidrotic ectodermal dysplasia.
    de Aquino SN; Paranaíba LM; Swerts MS; Martelli DR; de Barros LM; Martelli Júnior H
    Head Neck Pathol; 2012 Dec; 6(4):460-6. PubMed ID: 22421994
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia.
    Chassaing N; Bourthoumieu S; Cossee M; Calvas P; Vincent MC
    Hum Mutat; 2006 Mar; 27(3):255-9. PubMed ID: 16435307
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.