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PUBMED FOR HANDHELDS

Journal Abstract Search


117 related items for PubMed ID: 1666678

  • 1. [Genetic aspects in Klippel-Trenaunay syndrome].
    Aelvoet GE, Jorens PG, Roelen LM.
    Phlebologie; 1991; 44(4):809-14. PubMed ID: 1666678
    [Abstract] [Full Text] [Related]

  • 2. Genetic aspects of the Klippel-Trenaunay syndrome.
    Aelvoet GE, Jorens PG, Roelen LM.
    Br J Dermatol; 1992 Jun; 126(6):603-7. PubMed ID: 1319193
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  • 3. Some twin spots may not be twins.
    van Steensel MA.
    Am J Med Genet A; 2005 Feb 15; 133A(1):113. PubMed ID: 15633168
    [No Abstract] [Full Text] [Related]

  • 4. Brief communication: nevus unis lateris and Klippel-Trenaunay-Weber syndrome with the Sturge Weber anomalady in a consanguineous Puerto Rican family.
    Rivera-Reyes LR, Toro-Solá MA.
    Bol Asoc Med P R; 1979 Feb 15; 71(2):69-71. PubMed ID: 222308
    [No Abstract] [Full Text] [Related]

  • 5. A new case of Klippel-Trenaunay-Weber (KTW) syndrome: evidence of autosomal dominant inheritance.
    Ceballos-Quintal JM, Pinto-Escalante D, Castillo-Zapata I.
    Am J Med Genet; 1996 Jun 14; 63(3):426-7. PubMed ID: 8737646
    [Abstract] [Full Text] [Related]

  • 6. [Klippel-Trénaunay-Weber syndrome].
    Chessa Ricotti G, Giambi F, Martini R, Pietraperzia M.
    Pediatr Med Chir; 1984 Jun 14; 6(4):569-71. PubMed ID: 6099889
    [Abstract] [Full Text] [Related]

  • 7. [Clinical and genetic characteristics of the Klippel-Trenaunay syndrome].
    Kuklík M, Krejcík J, Marík J.
    Cas Lek Cesk; 1990 Sep 07; 129(36):1133-7. PubMed ID: 2171774
    [Abstract] [Full Text] [Related]

  • 8. Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocation.
    Whelan AJ, Watson MS, Porter FD, Steiner RD.
    Am J Med Genet; 1995 Dec 04; 59(4):492-4. PubMed ID: 8585570
    [Abstract] [Full Text] [Related]

  • 9. [Cobb syndrome and Klippel-Trenaunay-Weber syndrome].
    Fukutake T, Kawamura M, Moroo I, Asahina M, Hirayama K.
    Rinsho Shinkeigaku; 1991 Mar 04; 31(3):275-9. PubMed ID: 1654237
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  • 14. Klippel-Trenaunay syndrome in a monozygotic male twin: supportive evidence for the concept of paradominant inheritance.
    Hofer T, Frank J, Itin PH.
    Eur J Dermatol; 2005 Mar 04; 15(5):341-3. PubMed ID: 16172041
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  • 17. [Proteus syndrome. Expansion of the phenotype. Apropos of 3 pediatric cases].
    Hulsmans RF, Schrander-Stumpel CR, Koopman RJ, Hoorntje TM, Starink TM.
    Phlebologie; 1992 Mar 04; 45(4):463-9. PubMed ID: 1338804
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  • 19. Klippel-Trenaunay--Weber syndrome.
    Ofodile FA.
    East Afr Med J; 1981 Apr 04; 58(4):298-302. PubMed ID: 6266801
    [No Abstract] [Full Text] [Related]

  • 20. Klippel-Trenaunay syndrome: incidence and treatment of genitourinary sequelae.
    Husmann DA, Rathburn SR, Driscoll DJ.
    J Urol; 2007 Apr 04; 177(4):1244-9. PubMed ID: 17382698
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