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Journal Abstract Search

365 related items for PubMed ID: 10830910

  • 1. Genotype-phenotype correlations in families with deletions in the von Hippel-Lindau (VHL) gene.
    Hes F, Zewald R, Peeters T, Sijmons R, Links T, Verheij J, Matthijs G, Leguis E, Mortier G, van der Torren K, Rosman M, Lips C, Pearson P, van der Luijt R.
    Hum Genet; 2000 Apr; 106(4):425-31. PubMed ID: 10830910
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  • 3. Genotype-phenotype correlation in von Hippel-Lindau syndrome.
    Friedrich CA.
    Hum Mol Genet; 2001 Apr; 10(7):763-7. PubMed ID: 11257110
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  • 4. 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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  • 8. Genotype-phenotype correlations, and retinal function and structure in von Hippel-Lindau disease.
    Wittström E, Nordling M, Andréasson S.
    Ophthalmic Genet; 2014 Jun 01; 35(2):91-106. PubMed ID: 24555745
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  • 10. Novel and recurrent germline mutations in the VHL gene in 5 Arab patients with Von Hippel-Lindau disease.
    Faiyaz-Ul-Haque M, Jamil M, Aslam M, Abalkhail H, Al-Dayel F, Basit S, Nawaz Z, Zaidi SHE.
    Cancer Genet; 2020 May 01; 243():1-6. PubMed ID: 32179488
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  • 11. von Hippel-Lindau protein mutants linked to type 2C VHL disease preserve the ability to downregulate HIF.
    Hoffman MA, Ohh M, Yang H, Klco JM, Ivan M, Kaelin WG.
    Hum Mol Genet; 2001 May 01; 10(10):1019-27. PubMed ID: 11331612
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  • 12. Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.
    Zbar B, Kishida T, Chen F, Schmidt L, Maher ER, Richards FM, Crossey PA, Webster AR, Affara NA, Ferguson-Smith MA, Brauch H, Glavac D, Neumann HP, Tisherman S, Mulvihill JJ, Gross DJ, Shuin T, Whaley J, Seizinger B, Kley N, Olschwang S, Boisson C, Richard S, Lips CH, Lerman M.
    Hum Mutat; 1996 May 01; 8(4):348-57. PubMed ID: 8956040
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  • 18. [Von Hippel-Lindau disease].
    Shuin T, Ashida S, Yao M, Kanno H.
    Nihon Rinsho; 2000 Jul 01; 58(7):1448-54. PubMed ID: 10921322
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  • 19. Germline mutations in the von Hippel-Lindau (VHL) gene in patients from Poland: disease presentation in patients with deletions of the entire VHL gene.
    Cybulski C, Krzystolik K, Murgia A, Górski B, Debniak T, Jakubowska A, Martella M, Kurzawski G, Prost M, Kojder I, Limon J, Nowacki P, Sagan L, Białas B, Kałuza J, Zdunek M, Omulecka A, Jaskólski D, Kostyk E, Koraszewska-Matuszewska B, Haus O, Janiszewska H, Pecold K, Starzycka M, Słomski R, Cwirko M, Sikorski A, Gliniewicz B, Cyryłowski L, Fiszer-Maliszewska Ł, Gronwald J, Tołoczko-Grabarek A, Zajaczek S, Lubiński J.
    J Med Genet; 2002 Jul 01; 39(7):E38. PubMed ID: 12114495
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  • 20. The impact of molecular genetic analysis of the VHL gene in patients with haemangioblastomas of the central nervous system.
    Gläsker S, Bender BU, Apel TW, Natt E, van Velthoven V, Scheremet R, Zentner J, Neumann HP.
    J Neurol Neurosurg Psychiatry; 1999 Dec 01; 67(6):758-62. PubMed ID: 10567493
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