BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 12419039)

  • 21. 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]  

  • 22. Molecular and clinical study of familial adenomatous polyposis for genetic testing and management.
    Li G; Tamura K; Yamamoto Y; Sashio H; Utsunomiya J; Yamamura T; Shimoyama T; Furuyama J
    J Exp Clin Cancer Res; 1999 Dec; 18(4):519-29. PubMed ID: 10746979
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.
    Dommering CJ; Henneman L; van der Hout AH; Jonker MA; Tops CM; van den Ouweland AM; van der Luijt RB; Mensenkamp AR; Hogervorst FB; Redeker EJ; de Die-Smulders CE; Moll AC; Meijers-Heijboer H
    Fam Cancer; 2017 Apr; 16(2):271-277. PubMed ID: 27826806
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Preimplantation genetic diagnosis (PGD) for cancer predisposition syndromes].
    Malcov M; Ben-Yosef D; Amit A; Yaron Y
    Harefuah; 2011 Jun; 150(6):496-501, 553. PubMed ID: 21800485
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The most frequent APC mutations among Slovak familial adenomatous polyposis patients. Adenomatous polyposis coli.
    Zajac V; Kovác M; Kirchhoff T; Stevurková V; Tomka M
    Neoplasma; 2002; 49(6):356-61. PubMed ID: 12584582
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Hereditary cancer predisposition syndromes and preimplantation genetic diagnosis: where are we now?
    Konstantopoulou I; Pertesi M; Fostira F; Grivas A; Yannoukakos D
    J BUON; 2009 Sep; 14 Suppl 1():S187-92. PubMed ID: 19785065
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Preimplantation genetic diagnosis and monogenic inherited eye diseases].
    Hlavatá L; Ďuďáková Ľ; Trková M; Soldátová I; Skalická P; Kousal B; Lišková P
    Cesk Slov Oftalmol; 2016; 72(5):167-171. PubMed ID: 28224801
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Preimplantation genetic diagnosis as a strategy to prevent having a child born with an heritable eye disease.
    Yahalom C; Macarov M; Lazer-Derbeko G; Altarescu G; Imbar T; Hyman JH; Eldar-Geva T; Blumenfeld A
    Ophthalmic Genet; 2018 Aug; 39(4):450-456. PubMed ID: 29781739
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Detection of APC gene deletion by double competitive polymerase chain reaction in patients with familial adenomatous polyposis.
    Takahashi M; Kikuchi M; Ohkura N; Yaguchi H; Nagamura Y; Ohnami S; Ushiama M; Yoshida T; Sugano K; Iwama T; Kosugi S; Tsukada T
    Int J Oncol; 2006 Aug; 29(2):413-21. PubMed ID: 16820884
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Clinical analysis of preimplantation genetic diagnosis with HLA matching for beta-thalassemia].
    Liu XY; Wang J; Zeng YH; Ding CH; Shen XT; Zhou W; Li R; Zhou CQ; Xu YW
    Zhonghua Fu Chan Ke Za Zhi; 2016 Jul; 51(7):491-7. PubMed ID: 27465867
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [From gene to disease; Von Hippel-Lindau disease].
    Hes FJ; Los M; van der Luijt RB
    Ned Tijdschr Geneeskd; 2002 Jul; 146(29):1364-7. PubMed ID: 12162174
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Prenatal exclusion of von Hippel-Lindau syndrome in a Mexican family carrying a novel VHL gene mutation].
    Chacón-Camacho OF; Benitez-Granados J; Zenteno JC
    Ginecol Obstet Mex; 2014 Mar; 82(3):163-9. PubMed ID: 24779271
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Birth incidence and prevalence of tumor-prone syndromes: estimates from a UK family genetic register service.
    Evans DG; Howard E; Giblin C; Clancy T; Spencer H; Huson SM; Lalloo F
    Am J Med Genet A; 2010 Feb; 152A(2):327-32. PubMed ID: 20082463
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients.
    Mihalatos M; Apessos A; Dauwerse H; Velissariou V; Psychias A; Koliopanos A; Petropoulos K; Triantafillidis JK; Danielidis I; Fountzilas G; Agnantis NJ; Nasioulas G
    BMC Cancer; 2005 Apr; 5():40. PubMed ID: 15833136
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Prevention of familial tumor diseases using genetic counseling and early diagnosis].
    Müller H; Vasen HF
    Schweiz Med Wochenschr; 1990 Oct; 120(40):1451-60. PubMed ID: 1977199
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. A tale of four syndromes: familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome.
    Foulkes WD
    QJM; 1995 Dec; 88(12):853-63. PubMed ID: 8593545
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genetic basis of tumour development.
    Ponz de Leon M
    Ital J Gastroenterol; 1996 May; 28(4):232-45. PubMed ID: 8842841
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Preimplantation genetic diagnosis: state of the art.
    Basille C; Frydman R; El Aly A; Hesters L; Fanchin R; Tachdjian G; Steffann J; LeLorc'h M; Achour-Frydman N
    Eur J Obstet Gynecol Reprod Biol; 2009 Jul; 145(1):9-13. PubMed ID: 19411132
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Direct analysis for familial adenomatous polyposis mutations.
    Powell SM
    Mol Biotechnol; 2002 Feb; 20(2):197-207. PubMed ID: 11876475
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.