BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

275 related articles for article (PubMed ID: 28600700)

  • 1. Co-occurrence of Lynch syndrome and juvenile polyposis syndrome confirmed by multigene panel testing.
    Silva-Smith R; Sussman DA
    Fam Cancer; 2018 Jan; 17(1):87-90. PubMed ID: 28600700
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Exome sequencing in diagnostic evaluation of colorectal cancer predisposition in young patients.
    Tanskanen T; Gylfe AE; Katainen R; Taipale M; Renkonen-Sinisalo L; Mecklin JP; Järvinen H; Tuupanen S; Kilpivaara O; Vahteristo P; Aaltonen LA
    Scand J Gastroenterol; 2013 Jun; 48(6):672-8. PubMed ID: 23544471
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
    Rohlin A; Rambech E; Kvist A; Törngren T; Eiengård F; Lundstam U; Zagoras T; Gebre-Medhin S; Borg Å; Björk J; Nilbert M; Nordling M
    Fam Cancer; 2017 Apr; 16(2):195-203. PubMed ID: 27696107
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Rapid detection of germline mutations for hereditary gastrointestinal polyposis/cancers using HaloPlex target enrichment and high-throughput sequencing technologies.
    Kohda M; Kumamoto K; Eguchi H; Hirata T; Tada Y; Tanakaya K; Akagi K; Takenoshita S; Iwama T; Ishida H; Okazaki Y
    Fam Cancer; 2016 Oct; 15(4):553-62. PubMed ID: 26837502
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
    Yurgelun MB; Allen B; Kaldate RR; Bowles KR; Judkins T; Kaushik P; Roa BB; Wenstrup RJ; Hartman AR; Syngal S
    Gastroenterology; 2015 Sep; 149(3):604-13.e20. PubMed ID: 25980754
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial colorectal cancer.
    Lung MS; Trainer AH; Campbell I; Lipton L
    Intern Med J; 2015 May; 45(5):482-91. PubMed ID: 25955461
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lynch syndrome and MYH-associated polyposis: review and testing strategy.
    Goodenberger M; Lindor NM
    J Clin Gastroenterol; 2011 Jul; 45(6):488-500. PubMed ID: 21325953
    [TBL] [Abstract][Full Text] [Related]  

  • 9. ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
    Syngal S; Brand RE; Church JM; Giardiello FM; Hampel HL; Burt RW;
    Am J Gastroenterol; 2015 Feb; 110(2):223-62; quiz 263. PubMed ID: 25645574
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of coding exon 3 duplication in the BMPR1A gene in a patient with juvenile polyposis syndrome.
    Yamaguchi J; Nagayama S; Chino A; Sakata A; Yamamoto N; Sato Y; Ashihara Y; Kita M; Nomura S; Ishikawa Y; Igarashi M; Ueno M; Arai M
    Jpn J Clin Oncol; 2014 Oct; 44(10):1004-8. PubMed ID: 25129392
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Juvenile polyposis syndrome might be misdiagnosed as familial adenomatous polyposis: a case report and literature review.
    Gao XH; Li J; Zhao ZY; Xu XD; Du YQ; Yan HL; Liu LJ; Bai CG; Zhang W
    BMC Gastroenterol; 2020 Jun; 20(1):167. PubMed ID: 32487124
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer.
    Carethers JM; Stoffel EM
    World J Gastroenterol; 2015 Aug; 21(31):9253-61. PubMed ID: 26309352
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pathology and genetics of hereditary colorectal cancer.
    Ma H; Brosens LAA; Offerhaus GJA; Giardiello FM; de Leng WWJ; Montgomery EA
    Pathology; 2018 Jan; 50(1):49-59. PubMed ID: 29169633
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer].
    Jelsig AM; Tørring PM; Qvist N; Bernstein I; Ousager LB
    Ugeskr Laeger; 2013 Nov; 175(47A):. PubMed ID: 25353092
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Juvenile polyposis syndrome is a rare cause of gastrointestinal cancer].
    Jelsig AM; Tørring PM; Qvist N; Bernstein I; Ousager LB
    Ugeskr Laeger; 2014 Oct; 176(44):. PubMed ID: 25354001
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis-like phenotype and early onset cancer.
    Levi Z; Kariv R; Barnes-Kedar I; Goldberg Y; Half E; Morgentern S; Eli B; Baris HN; Vilkin A; Belfer RG; Niv Y; Elhasid R; Dvir R; Abu-Freha N; Cohen S
    Clin Genet; 2015 Nov; 88(5):474-8. PubMed ID: 25307252
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Targeted Next-Generation Sequencing for Hereditary Cancer Syndromes: A Focus on Lynch Syndrome and Associated Endometrial Cancer.
    Tafe LJ
    J Mol Diagn; 2015 Sep; 17(5):472-82. PubMed ID: 26162329
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.
    van der Klift HM; Mensenkamp AR; Drost M; Bik EC; Vos YJ; Gille HJ; Redeker BE; Tiersma Y; Zonneveld JB; García EG; Letteboer TG; Olderode-Berends MJ; van Hest LP; van Os TA; Verhoef S; Wagner A; van Asperen CJ; Ten Broeke SW; Hes FJ; de Wind N; Nielsen M; Devilee P; Ligtenberg MJ; Wijnen JT; Tops CM
    Hum Mutat; 2016 Nov; 37(11):1162-1179. PubMed ID: 27435373
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A young man with intestinal polyposis and epistaxis].
    Menko FH; Jacobs MA; Mager JJ; Nicolaï JJ; Mensenkamp AR; Aalfs CM
    Ned Tijdschr Geneeskd; 2014; 158():A7398. PubMed ID: 25269631
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cancer within the family tree: risks, diagnosis and treatment of juvenile polyposis syndrome.
    Kozacek K; Santos RL; Abdo M; Manibusan PA
    BMJ Case Rep; 2020 Aug; 13(8):. PubMed ID: 32816937
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.