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Journal Abstract Search

635 related items for PubMed ID: 10612832

  • 1. Somatic mosaicism in von Hippel-Lindau Disease.
    Murgia A, Martella M, Vinanzi C, Polli R, Perilongo G, Opocher G.
    Hum Mutat; 2000 Jan; 15(1):114. PubMed ID: 10612832
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  • 3. von Hippel-Lindau disease.
    Couch V, Lindor NM, Karnes PS, Michels VV.
    Mayo Clin Proc; 2000 Mar; 75(3):265-72. PubMed ID: 10725953
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  • 4. Molecular characterization and ophthalmic investigation of a large family with type 2A Von Hippel-Lindau Disease.
    Allen RC, Webster AR, Sui R, Brown J, Taylor CM, Stone EM.
    Arch Ophthalmol; 2001 Nov; 119(11):1659-65. PubMed ID: 11709017
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  • 6. Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas.
    Dannenberg H, De Krijger RR, van der Harst E, Abbou M, IJzendoorn Y, Komminoth P, Dinjens WN.
    Int J Cancer; 2003 Jun 10; 105(2):190-5. PubMed ID: 12673678
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  • 8. Variable penetrance of familial pheochromocytoma associated with the von Hipple Lindau gene mutation, S68W. Mutations in brief no. 150. Online.
    Martin R, Hockey A, Walpole I, Goldblatt J.
    Hum Mutat; 1998 Jun 10; 12(1):71. PubMed ID: 10627136
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  • 9. DNA-based diagnosis of the von Hippel-Lindau syndrome.
    Patel RJ, Appukuttan B, Ott S, Wang X, Stout JT.
    Am J Ophthalmol; 2000 Feb 10; 129(2):258-60. PubMed ID: 10682986
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  • 10. Von Hippel-Lindau syndrome. A pleomorphic condition.
    Friedrich CA.
    Cancer; 1999 Dec 01; 86(11 Suppl):2478-82. PubMed ID: 10630173
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  • 11. Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors.
    Prowse AH, Webster AR, Richards FM, Richard S, Olschwang S, Resche F, Affara NA, Maher ER.
    Am J Hum Genet; 1997 Apr 01; 60(4):765-71. PubMed ID: 9106522
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  • 12. [Von Hippel-Lindau syndrome with spinal, cerebellar, and retinal hemangioblastoma in identical twins].
    Wessels T, Kemeny S, Block F.
    Nervenarzt; 2002 Dec 01; 73(12):1195-8. PubMed ID: 12486572
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  • 13. Multiple intracerebral haemangioblastomas in identical twins with von Hippel-Lindau disease--a clinical and molecular study.
    Sobottka SB, Frank S, Hampl M, Schackert HK, Schackert G.
    Acta Neurochir (Wien); 1998 Dec 01; 140(3):281-5. PubMed ID: 9638266
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  • 14. Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system.
    Gläsker S, Bender BU, Apel TW, van Velthoven V, Mulligan LM, Zentner J, Neumann HP.
    J Neurol Neurosurg Psychiatry; 2001 May 01; 70(5):644-8. PubMed ID: 11309459
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  • 15. Somatic von Hippel-Lindau gene mutations detected in sporadic endolymphatic sac tumors.
    Vortmeyer AO, Huang SC, Koch CA, Governale L, Dickerman RD, McKeever PE, Oldfield EH, Zhuang Z.
    Cancer Res; 2000 Nov 01; 60(21):5963-5. PubMed ID: 11085513
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  • 16. Retinal abnormalities associated with a mutation of the nucleotide 683 in von Hippel-Lindau disease.
    Piermarocchi S, Lo Giudice G, Pilotto E, Bertoja E, Scaroni C, Martella M, Opocher G, Murgia A.
    Graefes Arch Clin Exp Ophthalmol; 2000 Jul 01; 238(7):615-20. PubMed ID: 10955664
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  • 17. Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.
    Maher ER, Webster AR, Richards FM, Green JS, Crossey PA, Payne SJ, Moore AT.
    J Med Genet; 1996 Apr 01; 33(4):328-32. PubMed ID: 8730290
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  • 18. Von Hippel-Lindau disease and sporadic renal cell carcinoma.
    Zbar B.
    Cancer Surv; 1995 Apr 01; 25():219-32. PubMed ID: 8718521
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  • 19. Genetic study of a large Chinese kindred with von Hippel-Lindau disease.
    Huang YR, Zhang J, Wang JD, Fan XD.
    Chin Med J (Engl); 2004 Apr 01; 117(4):552-7. PubMed ID: 15109448
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  • 20. von Hippel-Lindau disease type 2A in a family with a duplicated 21-base-pair in-frame insertion mutation in the VHL gene.
    Miyagawa Y, Nakazawa M, Noda Y, Ito S, Ohguro H.
    Graefes Arch Clin Exp Ophthalmol; 2003 Mar 01; 241(3):241-4. PubMed ID: 12644949
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