BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

736 related articles for article (PubMed ID: 8737656)

  • 1. Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child.
    Moerman P; Fryns JP
    Am J Med Genet; 1996 Jun; 63(3):479-81. PubMed ID: 8737656
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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]  

  • 3. [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]  

  • 4. A 19-year follow-up of a patient with type 3 ectrodactyly-ectodermal dysplasia-clefting syndrome who developed non-Hodgkin lymphoma.
    Balci S; Engiz O; Okten G; Sipahier M; Gursu G; Kandemir B
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Sep; 108(3):e91-5. PubMed ID: 19716498
    [TBL] [Abstract][Full Text] [Related]  

  • 5. EEC syndrome: report on 20 new patients, clinical and genetic considerations.
    Rodini ES; Richieri-Costa A
    Am J Med Genet; 1990 Sep; 37(1):42-53. PubMed ID: 2240042
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genitourinary anomalies are a component manifestation in the ectodermal dysplasia, ectrodactyly, cleft lip/palate (EEC) syndrome.
    Rollnick BR; Hoo JJ
    Am J Med Genet; 1988 Jan; 29(1):131-6. PubMed ID: 3278611
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Dysmaturity as symptom of the ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome].
    Porcelijn L; Maat-Kievit JA; van Haeringen A
    Tijdschr Kindergeneeskd; 1993 Jun; 61(3):96-9. PubMed ID: 8211943
    [TBL] [Abstract][Full Text] [Related]  

  • 8. EEC syndrome (ectrodactyly-ectodermal dysplasia-clefting): a clinical case report.
    Ulukapi I; Bilgin T; Yalçin S
    ASDC J Dent Child; 2001; 68(5-6):350-2, 302. PubMed ID: 11985198
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Adipsic hypernatremia and bilateral renal stones in a child with ectrodactyly-ectodermal dysplasia-cleft lip-palate (EEC) syndrome.
    Shawky RM; Elsayed SM; Sadik DI; Gad S; Seifeldin NS
    Genet Couns; 2010; 21(2):215-20. PubMed ID: 20681222
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [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]  

  • 13. Ectrodactary, ectodermal dysplasia, and cleft lip-palate syndrome.
    Choong YY; Norazlina B
    Med J Malaysia; 2001 Mar; 56(1):88-91. PubMed ID: 11503303
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome: dominant inheritance and variable expression.
    Penchaszadeh VB; de Negrotti TC
    J Med Genet; 1976 Aug; 13(4):281-4. PubMed ID: 957377
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rapp-Hodgkin syndrome: report of a Brazilian family.
    Rodini EO; Freitas JA; Richieri-Costa A
    Am J Med Genet; 1990 Aug; 36(4):463-6. PubMed ID: 2389804
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA-binding domain of the TP63 gene and genotype-phenotype correlation.
    Clements SE; Techanukul T; Coman D; Mellerio JE; McGrath JA
    Br J Dermatol; 2010 Jan; 162(1):201-7. PubMed ID: 19903181
    [TBL] [Abstract][Full Text] [Related]  

  • 18. R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy.
    Valenzise M; Arrigo T; De Luca F; Privitera A; Frigiola A; Carando A; Garelli E; Silengo M
    Eur J Med Genet; 2008; 51(5):497-500. PubMed ID: 18603493
    [TBL] [Abstract][Full Text] [Related]  

  • 19. EC syndrome in a girl with paracentric inversion (7)(q22.1;q36.3).
    Akita S; Kuratomi H; Abe K; Harada N; Mukae N; Niikawa N
    Clin Dysmorphol; 1993 Jan; 2(1):62-7. PubMed ID: 8298740
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of Goltz-Gorlin syndrome versus EEC syndrome.
    Rodini ES; Nardi A; Guion-Almeida ML; Richieri-Costa A
    Am J Med Genet; 1992 Feb; 42(3):276-80. PubMed ID: 1536161
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 37.