BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 24460914)

  • 1. Limited ectrodactyly, ectodermal dysplasia and cleft lip-palate syndrome with a p63 mutation, associated with linear and whorled naevoid hypermelanosis.
    Pratsou P; Defty CL; Ozoemena L; McGrath JA; Moss C; Gach JE
    Clin Exp Dermatol; 2014 Mar; 39(2):266-8. PubMed ID: 24460914
    [No Abstract]   [Full Text] [Related]  

  • 2. Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype.
    Paranaíba LM; Martelli-Júnior H; de Miranda RT; Bufalino A; Abdo Filho RC; Coletta RD
    Cleft Palate Craniofac J; 2010 Sep; 47(5):544-7. PubMed ID: 20180707
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ectrodactyly-ectodermal dysplasia-cleft syndrome (EEC syndrome) with a developmental delay caused by R304W mutation in the tp63 gene.
    Gawrych E; Bińczak-Kuleta A; Janiszewska-Olszowska J; Ciechanowicz A
    Ann Acad Med Stetin; 2013; 59(1):11-4. PubMed ID: 24734328
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Ectrodactyly, ectodermal dysplasia, cleft lip and palate syndrome (EEC syndrome)].
    Ostorharics-Horváth G; Lázár I
    Orv Hetil; 1989 Oct; 130(41):2211-2. PubMed ID: 2812754
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sweating ability of patients with p63-associated syndromes.
    Ferstl P; Wohlfart S; Schneider H
    Eur J Pediatr; 2018 Nov; 177(11):1727-1731. PubMed ID: 30088137
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case of ankyloblepharon, ectodermal dysplasia, and cleft lip/palate syndrome with ectrodactyly: are the p63 syndromes distinct after all?
    Chiu YE; Drolet BA; Duffy KJ; Holland KE
    Pediatr Dermatol; 2011; 28(1):15-9. PubMed ID: 19793345
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Ectrodactyly, ectodermal dysplasia, and cleft lip and palate: an hereditary syndrome with an autosomal dominant mode of inheritance (author's transl)].
    Pfeiffer RA; Verbeck C
    Z Kinderheilkd; 1973 Oct; 115(3):235-44. PubMed ID: 4801123
    [No Abstract]   [Full Text] [Related]  

  • 8. De novo missense mutation, S541Y, in the p63 gene underlying Rapp-Hodgkin ectodermal dysplasia syndrome.
    Shotelersuk V; Janklat S; Siriwan P; Tongkobpetch S
    Clin Exp Dermatol; 2005 May; 30(3):282-5. PubMed ID: 15807690
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Skin erosions and wound healing in ankyloblepharon-ectodermal defect-cleft lip and/or palate.
    Siegfried E; Bree A; Fete M; Sybert VP
    Arch Dermatol; 2005 Dec; 141(12):1591-4. PubMed ID: 16365264
    [No Abstract]   [Full Text] [Related]  

  • 10. [Ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome, report of a case with variable expressivity].
    Meza Escobar LE; Isaza C; Pachajoa H
    Arch Argent Pediatr; 2012 Oct; 110(5):e95-8. PubMed ID: 23070194
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ectrodactyly, ectodermal dysplasia, cleft lip and palate (EEC)--a rare syndrome.
    Parkash H; Grewal MS; Sidhu SS
    Indian J Pediatr; 1983; 50(404):337-40. PubMed ID: 6668041
    [No Abstract]   [Full Text] [Related]  

  • 12. Ectodermal dysplasia, ectrodactyly, cleft lip/palate syndrome without ectrodactyly.
    Sankhyan N; Kaushal RK; Sarin S
    Dermatol Online J; 2006 May; 12(4):5. PubMed ID: 17083860
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ectrodactyly-ectodermal dysplasia-cleft lip and palate syndrome in twins.
    Kogan L; Ariely D; Kapitulsky L; Govrin-Yehudain J
    Ann Plast Surg; 2001 Nov; 47(5):580-1. PubMed ID: 11716280
    [No Abstract]   [Full Text] [Related]  

  • 14. [Familial split hand and foot, cleft lip and palate, ectodermal dysplasia syndrome].
    Szappanos L; Czeizel E; Szepesi K
    Orv Hetil; 1984 Mar; 125(11):633-8. PubMed ID: 6700970
    [No Abstract]   [Full Text] [Related]  

  • 15. A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting.
    Sorasio L; Biamino E; Garelli E; Ferrero GB; Silengo MC
    Clin Exp Dermatol; 2009 Dec; 34(8):e726-8. PubMed ID: 19663851
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rapp-Hodgkin and Hay-Wells ectodermal dysplasia syndromes represent a variable spectrum of the same genetic disorder.
    Clements SE; Techanukul T; Holden ST; Mellerio JE; Dorkins H; Escande F; McGrath JA
    Br J Dermatol; 2010 Sep; 163(3):624-9. PubMed ID: 20491771
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spectrum of p63 mutations in a selected patient cohort affected with ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (AEC).
    Rinne T; Bolat E; Meijer R; Scheffer H; van Bokhoven H
    Am J Med Genet A; 2009 Sep; 149A(9):1948-51. PubMed ID: 19676060
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hay-Wells syndrome in a child with mutation in the TP73L gene.
    Garcia Bartels N; Neumann LM; Mleczko A; Rubach K; Peters H; Rossi R; Sterry W; Blume-Peytavi U
    J Dtsch Dermatol Ges; 2007 Oct; 5(10):919-23. PubMed ID: 17910675
    [TBL] [Abstract][Full Text] [Related]  

  • 19. AEC syndrome: further evidence of a common genetic etiology with Rapp-Hodgkin syndrome.
    Sorasio L; Ferrero GB; Garelli E; Brunello G; Martano C; Carando A; Belligni E; Dianzani I; Cirillo Silengo M
    Eur J Med Genet; 2006; 49(6):520-2. PubMed ID: 16824815
    [No Abstract]   [Full Text] [Related]  

  • 20. [Ectodactylia-ectodermal dysplasia, cleft lip, jaw and palate syndrome (EEC syndrome). Association with van der Woude syndrome?].
    Haensch R; Küster W; Hammerstein W
    Dtsch Z Mund Kiefer Gesichtschir; 1985; 9(3):225-6. PubMed ID: 3868444
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.