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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

170 related items for PubMed ID: 9781908

  • 1. Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome.
    Neri G, Gurrieri F, Zanni G, Lin A.
    Am J Med Genet; 1998 Oct 02; 79(4):279-83. PubMed ID: 9781908
    [Abstract] [Full Text] [Related]

  • 2. GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome.
    Li M, Shuman C, Fei YL, Cutiongco E, Bender HA, Stevens C, Wilkins-Haug L, Day-Salvatore D, Yong SL, Geraghty MT, Squire J, Weksberg R.
    Am J Med Genet; 2001 Aug 01; 102(2):161-8. PubMed ID: 11477610
    [Abstract] [Full Text] [Related]

  • 3. Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome.
    Pilia G, Hughes-Benzie RM, MacKenzie A, Baybayan P, Chen EY, Huber R, Neri G, Cao A, Forabosco A, Schlessinger D.
    Nat Genet; 1996 Mar 01; 12(3):241-7. PubMed ID: 8589713
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature.
    Garganta CL, Bodurtha JN.
    Am J Med Genet; 1992 Sep 15; 44(2):129-35. PubMed ID: 1456279
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Simpson Golabi Behmel syndrome: progress toward understanding the molecular basis for overgrowth, malformation, and cancer predisposition.
    DeBaun MR, Ess J, Saunders S.
    Mol Genet Metab; 2001 Apr 15; 72(4):279-86. PubMed ID: 11286501
    [Abstract] [Full Text] [Related]

  • 8. Clinical and molecular studies on two further families with Simpson-Golabi-Behmel syndrome.
    Rodríguez-Criado G, Magano L, Segovia M, Gurrieri F, Neri G, González-Meneses A, Gómez de Terreros I, Valdéz R, Gracia R, Lapunzina P.
    Am J Med Genet A; 2005 Oct 15; 138A(3):272-7. PubMed ID: 16158429
    [Abstract] [Full Text] [Related]

  • 9. Simpson-Golabi-Behmel syndrome.
    Vaisfeld A, Neri G.
    Am J Med Genet C Semin Med Genet; 2024 Dec 15; 196(4):e32088. PubMed ID: 38766979
    [Abstract] [Full Text] [Related]

  • 10. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development].
    Weidle B, Orstavik KH.
    Tidsskr Nor Laegeforen; 1998 Apr 20; 118(10):1556-8. PubMed ID: 9615582
    [Abstract] [Full Text] [Related]

  • 11. Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndrome.
    Cano-Gauci DF, Song HH, Yang H, McKerlie C, Choo B, Shi W, Pullano R, Piscione TD, Grisaru S, Soon S, Sedlackova L, Tanswell AK, Mak TW, Yeger H, Lockwood GA, Rosenblum ND, Filmus J.
    J Cell Biol; 1999 Jul 12; 146(1):255-64. PubMed ID: 10402475
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations.
    Yano S, Baskin B, Bagheri A, Watanabe Y, Moseley K, Nishimura A, Matsumoto N, Ray PN.
    Clin Genet; 2011 Nov 12; 80(5):466-71. PubMed ID: 20950395
    [Abstract] [Full Text] [Related]

  • 14. Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: patient report and review of the literature.
    Mariani S, Iughetti L, Bertorelli R, Coviello D, Pellegrini M, Forabosco A, Bernasconi S.
    J Pediatr Endocrinol Metab; 2003 Feb 12; 16(2):225-32. PubMed ID: 12713262
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
    Gurrieri F, Cappa M, Neri G.
    Am J Med Genet; 1992 Sep 15; 44(2):136-7. PubMed ID: 1456280
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. GPC3 mutations in seven patients with Simpson-Golabi-Behmel syndrome.
    Sakazume S, Okamoto N, Yamamoto T, Kurosawa K, Numabe H, Ohashi Y, Kako Y, Nagai T, Ohashi H.
    Am J Med Genet A; 2007 Aug 01; 143A(15):1703-7. PubMed ID: 17603795
    [Abstract] [Full Text] [Related]

  • 19. Mutational analysis of the GPC3/GPC4 glypican gene cluster on Xq26 in patients with Simpson-Golabi-Behmel syndrome: identification of loss-of-function mutations in the GPC3 gene.
    Veugelers M, Cat BD, Muyldermans SY, Reekmans G, Delande N, Frints S, Legius E, Fryns JP, Schrander-Stumpel C, Weidle B, Magdalena N, David G.
    Hum Mol Genet; 2000 May 22; 9(9):1321-8. PubMed ID: 10814714
    [Abstract] [Full Text] [Related]

  • 20. Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.
    Terespolsky D, Farrell SA, Siegel-Bartelt J, Weksberg R.
    Am J Med Genet; 1995 Nov 20; 59(3):329-33. PubMed ID: 8599356
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.