BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 33849326)

  • 61. [Clinical features and current progress of familial adenomatous polyposis].
    Ushio K
    Nihon Rinsho; 2000 Jul; 58(7):1385-95. PubMed ID: 10921310
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Extra-intestinal manifestations of familial adenomatous polyposis.
    Groen EJ; Roos A; Muntinghe FL; Enting RH; de Vries J; Kleibeuker JH; Witjes MJ; Links TP; van Beek AP
    Ann Surg Oncol; 2008 Sep; 15(9):2439-50. PubMed ID: 18612695
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Genetic testing and phenotype in a large kindred with attenuated familial adenomatous polyposis.
    Burt RW; Leppert MF; Slattery ML; Samowitz WS; Spirio LN; Kerber RA; Kuwada SK; Neklason DW; Disario JA; Lyon E; Hughes JP; Chey WY; White RL
    Gastroenterology; 2004 Aug; 127(2):444-51. PubMed ID: 15300576
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Gene variants associated to malignant thyroid disease in familial adenomatous polyposis: a novel APC germline mutation.
    Martayan A; Sanchez-Mete L; Baldelli R; Falvo E; Barnabei A; Conti L; Giacomini P; Appetecchia M; Stigliano V
    J Endocrinol Invest; 2010 Oct; 33(9):603-6. PubMed ID: 20935450
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Presence of c.3956delC mutation in familial adenomatous polyposis patients from Brazil.
    Moreira-Nunes CA; Alcântara Dd; Lima-Júnior SF; Cavalléro SR; Rey JA; Pinto GR; de Assumpção PP; Burbano RR
    World J Gastroenterol; 2015 Aug; 21(31):9413-9. PubMed ID: 26309368
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Multiple gynecologic tumors as rare associated phenotypes of FAP/Gardner syndrome in a family with the novel germline mutation in the APC gene.
    Kovac M; Tomka M; Ciernikova S; Stevurkova V; Valachova A; Zajac V
    Clin Genet; 2006 Feb; 69(2):183-6. PubMed ID: 16433700
    [No Abstract]   [Full Text] [Related]  

  • 67. [Familial polyposis coli].
    Watanabe T; Muto T
    Nihon Rinsho; 1995 Nov; 53(11):2722-7. PubMed ID: 8538033
    [TBL] [Abstract][Full Text] [Related]  

  • 68. ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).
    Hegde M; Ferber M; Mao R; Samowitz W; Ganguly A;
    Genet Med; 2014 Jan; 16(1):101-16. PubMed ID: 24310308
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes.
    Cruz-Correa M; Diaz-Algorri Y; Mendez V; Vazquez PJ; Lozada ME; Freyre K; Lathroum L; Gonzalez-Pons M; Hernandez-Marrero J; Giardiello F; Rodriguez-Quilichini S
    Fam Cancer; 2013 Sep; 12(3):555-62. PubMed ID: 23460355
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Mutation cluster region, association between germline and somatic mutations and genotype-phenotype correlation in upper gastrointestinal familial adenomatous polyposis.
    Groves C; Lamlum H; Crabtree M; Williamson J; Taylor C; Bass S; Cuthbert-Heavens D; Hodgson S; Phillips R; Tomlinson I
    Am J Pathol; 2002 Jun; 160(6):2055-61. PubMed ID: 12057910
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Gardener-associated fibroma: an unusual cause of upper airway obstruction.
    Pinto RS; Simons A; Verma R; Bateman N
    BMJ Case Rep; 2018 Sep; 2018():. PubMed ID: 30269086
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Importance of sessile serrated lesions in a patient with familial adenomatous polyposis.
    Watanabe M; Ishikawa H; Ishiguro S; Mutoh M
    Clin J Gastroenterol; 2021 Dec; 14(6):1667-1670. PubMed ID: 34455522
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Multiple nuchal fibromas in a 2-year-old without Gardner syndrome.
    LeBlanc KG; Wenner M; Davis LS
    Pediatr Dermatol; 2011; 28(6):695-696. PubMed ID: 21950671
    [TBL] [Abstract][Full Text] [Related]  

  • 74. [Familial adenomatous polyposis or Gardner syndrome--review of the literature and presentation of 2 clinical cases].
    Karazivan M; Manoukian K; Lalonde B
    J Can Dent Assoc; 2000 Jan; 66(1):26-30. PubMed ID: 10680330
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?
    Aretz S; Koch A; Uhlhaas S; Friedl W; Propping P; von Schweinitz D; Pietsch T
    Pediatr Blood Cancer; 2006 Nov; 47(6):811-8. PubMed ID: 16317745
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Identification of aggressive Gardner syndrome phenotype associated with a de novo
    Kiessling P; Dowling E; Huang Y; Ho ML; Balakrishnan K; Weigel BJ; Highsmith WE; Niu Z; Schimmenti LA
    Cold Spring Harb Mol Case Stud; 2019 Apr; 5(2):. PubMed ID: 30696621
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Preliminary results of the molecular diagnosis of familial adenomatous polyposis in Cuban families.
    Cruz-Bustillo D; Villasana L; Llorente F; Casadesús D; García E; Syrris P; Carter N; Guerra R; Llanio R
    Int J Colorectal Dis; 2002 Sep; 17(5):344-7. PubMed ID: 12172928
    [TBL] [Abstract][Full Text] [Related]  

  • 78. [Hereditary colorectal cancer].
    Park JG; Kim IJ
    Korean J Gastroenterol; 2005 Feb; 45(2):78-87. PubMed ID: 15725711
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Familial juvenile polyposis syndrome with a de novo germline missense variant in BMPR1A gene: a case report.
    Liu Q; Liu M; Liu T; Yu Y
    BMC Med Genet; 2020 Oct; 21(1):196. PubMed ID: 33032550
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel.
    Spier I; Yin X; Richardson M; Pineda M; Laner A; Ritter D; Boyle J; Mur P; Hansen TVO; Shi X; Mahmood K; Plazzer JP; Ognedal E; Nordling M; Farrington SM; Yamamoto G; Baert-Desurmont S; Martins A; Borras E; Tops C; Webb E; Beshay V; Genuardi M; Pesaran T; Capellá G; Tavtigian SV; Latchford A; Frayling IM; Plon SE; Greenblatt M; Macrae FA; Aretz S;
    Genet Med; 2024 Feb; 26(2):100992. PubMed ID: 37800450
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.