BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 19270817)

  • 1. Improved detection of germline mutations in Korean VHL patients by multiple ligation-dependent probe amplification analysis.
    Cho HJ; Ki CS; Kim JW
    J Korean Med Sci; 2009 Feb; 24(1):77-83. PubMed ID: 19270817
    [TBL] [Abstract][Full Text] [Related]  

  • 2. VHL Germline Mutations in Argentinian Patients with Clinical Diagnoses or Single Typical Manifestations of Type 1 von Hippel-Lindau Disease.
    Mathó C; Sansó G; Diez B; Barontini M; Pennisi PA
    Genet Test Mol Biomarkers; 2016 Dec; 20(12):771-776. PubMed ID: 27617348
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.
    Hes FJ; van der Luijt RB; Janssen AL; Zewald RA; de Jong GJ; Lenders JW; Links TP; Luyten GP; Sijmons RH; Eussen HJ; Halley DJ; Lips CJ; Pearson PL; van den Ouweland AM; Majoor-Krakauer DF
    Clin Genet; 2007 Aug; 72(2):122-9. PubMed ID: 17661816
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene.
    Stolle C; Glenn G; Zbar B; Humphrey JS; Choyke P; Walther M; Pack S; Hurley K; Andrey C; Klausner R; Linehan WM
    Hum Mutat; 1998; 12(6):417-23. PubMed ID: 9829911
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Germline mutations in the von Hippel-Lindau disease (VHL) gene in mainland Chinese families.
    Zhang J; Huang Y; Pan J; Liu D; Zhou L; Xue W; Chen Q; Dong B; Xuan H
    J Cancer Res Clin Oncol; 2008 Nov; 134(11):1211-8. PubMed ID: 18446368
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Family history of von Hippel-Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients.
    Wu P; Zhang N; Wang X; Ning X; Li T; Bu D; Gong K
    J Hum Genet; 2012 Apr; 57(4):238-43. PubMed ID: 22357542
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Large germline deletion of the VHL gene in Chinese families with von Hippel-Lindau syndrome].
    Zhang J; Chen HG; Xue W; Zhou LX; Huang YR
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):539-41. PubMed ID: 19806577
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Germline mutation of Glu70Lys is highly frequent in Korean patients with von Hippel-Lindau (VHL) disease.
    Hwang S; Ku CR; Lee JI; Hur KY; Lee MS; Lee CH; Koo KY; Lee JS; Rhee Y
    J Hum Genet; 2014 Sep; 59(9):488-93. PubMed ID: 25078357
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 243():1-6. PubMed ID: 32179488
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 67(6):758-62. PubMed ID: 10567493
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Associations between VHL genotype and clinical phenotype in familial von Hippel-Lindau disease.
    Huang JS; Huang CJ; Chen SK; Chien CC; Chen CW; Lin CM
    Eur J Clin Invest; 2007 Jun; 37(6):492-500. PubMed ID: 17537157
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.
    Gergics P; Patocs A; Toth M; Igaz P; Szucs N; Liko I; Fazakas F; Szabo I; Kovacs B; Glaz E; Racz K
    Eur J Endocrinol; 2009 Sep; 161(3):495-502. PubMed ID: 19574279
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Germline mutations of the VHL gene in seven Chinese families with von Hippel-Lindau disease.
    Huang Y; Zhou D; Liu J; Zhou P; Li X; Wang Z
    Int J Mol Med; 2012 Jan; 29(1):47-52. PubMed ID: 21972040
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotype-phenotype analysis of von Hippel-Lindau syndrome in Korean families: HIF-α binding site missense mutations elevate age-specific risk for CNS hemangioblastoma.
    Lee JS; Lee JH; Lee KE; Kim JH; Hong JM; Ra EK; Seo SH; Lee SJ; Kim MJ; Park SS; Seong MW
    BMC Med Genet; 2016 Jul; 17(1):48. PubMed ID: 27439424
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas.
    Kang HC; Kim IJ; Park JH; Shin Y; Jang SG; Ahn SA; Park HW; Lim SK; Oh SK; Kim DJ; Lee KW; Choi YS; Park YJ; Lee MR; Kim DW; Park JG
    Oncol Rep; 2005 Oct; 14(4):879-83. PubMed ID: 16142346
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation.
    Gomy I; Molfetta GA; de Andrade Barreto E; Ferreira CA; Zanette DL; Casali-da-Rocha JC; Silva WA
    Fam Cancer; 2010 Dec; 9(4):635-42. PubMed ID: 20567917
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype phenotype correlation in Asian Indian von Hippel-Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma.
    Lomte N; Kumar S; Sarathi V; Pandit R; Goroshi M; Jadhav S; Lila AR; Bandgar T; Shah NS
    Fam Cancer; 2018 Jul; 17(3):441-449. PubMed ID: 29124493
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 33(4):328-32. PubMed ID: 8730290
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular basis of von Hippel-Lindau syndrome in Chinese patients.
    Siu WK; Ma RC; Lam CW; Mak CM; Yuen YP; Lo FM; Chan KW; Lam SF; Ling SC; Tong SF; So WY; Chow CC; Tang MH; Tam WH; Chan AY
    Chin Med J (Engl); 2011 Jan; 124(2):237-41. PubMed ID: 21362373
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.