BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 8696342)

  • 21. Genetics of Wilms' tumor.
    Coppes MJ; Egeler RM
    Semin Urol Oncol; 1999 Feb; 17(1):2-10. PubMed ID: 10073400
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clonality and loss of heterozygosity of WT genes are early events in the pathogenesis of nephroblastomas.
    Guertl B; Ratschek M; Harms D; Jaenig U; Leuschner I; Poremba C; Hoefler G
    Hum Pathol; 2003 Mar; 34(3):278-81. PubMed ID: 12673563
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 16q loss of heterozygosity and microsatellite instability in Wilms' tumor.
    Mason JE; Goodfellow PJ; Grundy PE; Skinner MA
    J Pediatr Surg; 2000 Jun; 35(6):891-6; discussion 896-7. PubMed ID: 10873032
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetics of kidney tumours.
    Fleming S
    Forum (Genova); 1998; 8(2):176-84. PubMed ID: 9666053
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 16q heterozygosity loss in Wilms' tumour in children and its clinical importance.
    Skotnicka-Klonowicz G; Rieske P; Bartkowiak J; Szymik-Kantorowicz S; Daszkiewicz P; Debiec-Rychter M
    Eur J Surg Oncol; 2000 Feb; 26(1):61-6. PubMed ID: 10718182
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Fifth finger camptodactyly maps to chromosome 3q11.2-q13.12 in a large German kindred.
    Malik S; Schott J; Schiller J; Junge A; Baum E; Koch MC
    Eur J Hum Genet; 2008 Feb; 16(2):265-9. PubMed ID: 18000522
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Familial occurrence of nephroblastoma].
    Skotnicka-Klonowicz G; Rieske P; Bartkowiak J; Debiec-Rychter M
    Pol Merkur Lekarski; 2001 Feb; 10(56):96-7. PubMed ID: 11320587
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Familial predisposition to Wilms tumor does not segregate with the WT1 gene.
    Schwartz CE; Haber DA; Stanton VP; Strong LC; Skolnick MH; Housman DE
    Genomics; 1991 Aug; 10(4):927-30. PubMed ID: 1655633
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Loss of heterozygosity at chromosome 11p15 in Wilms tumors: identification of two independent regions.
    Karnik P; Chen P; Paris M; Yeger H; Williams BR
    Oncogene; 1998 Jul; 17(2):237-40. PubMed ID: 9674708
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mapping of an autosomal dominant gene for Dupuytren's contracture to chromosome 16q in a Swedish family.
    Hu FZ; Nystrom A; Ahmed A; Palmquist M; Dopico R; Mossberg I; Gladitz J; Rayner M; Post JC; Ehrlich GD; Preston RA
    Clin Genet; 2005 Nov; 68(5):424-9. PubMed ID: 16207209
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
    Gasser T; Müller-Myhsok B; Wszolek ZK; Oehlmann R; Calne DB; Bonifati V; Bereznai B; Fabrizio E; Vieregge P; Horstmann RD
    Nat Genet; 1998 Mar; 18(3):262-5. PubMed ID: 9500549
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Wilms' tumour: connecting tumorigenesis and organ development in the kidney.
    Rivera MN; Haber DA
    Nat Rev Cancer; 2005 Sep; 5(9):699-712. PubMed ID: 16110318
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetics of embryonal tumours of childhood: retinoblastoma, Wilms' tumour and neuroblastoma.
    Brodeur GM
    Cancer Surv; 1995; 25():67-99. PubMed ID: 8718513
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Familial extrarenal Wilms tumor.
    Houben CH; Tong JH; Chan AW; Chik KW; Lee KH; Sihoe JD; Tam YH; Yeung CK
    J Pediatr Surg; 2007 Nov; 42(11):1826-30. PubMed ID: 18022431
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q.
    Badenhop RF; Moses MJ; Scimone A; Mitchell PB; Ewen KR; Rosso A; Donald JA; Adams LJ; Schofield PR
    Mol Psychiatry; 2001 Jul; 6(4):396-403. PubMed ID: 11443523
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular analysis of E-cadherin and cadherin-11 in Wilms' tumours.
    Schulz S; Becker KF; Braungart E; Reichmuth C; Klamt B; Becker I; Atkinson M; Gessler M; Höfler H
    J Pathol; 2000 Jun; 191(2):162-9. PubMed ID: 10861576
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Familial predisposition to neuroblastoma does not map to chromosome band 1p36.
    Maris JM; Kyemba SM; Rebbeck TR; White PS; Sulman EP; Jensen SJ; Allen C; Biegel JA; Yanofsky RA; Feldman GL; Brodeur GM
    Cancer Res; 1996 Aug; 56(15):3421-5. PubMed ID: 8758905
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The expression pattern of Wilms' tumour gene (WT1) product in normal tissues and paediatric renal tumours.
    Ramani P; Cowell JK
    J Pathol; 1996 Jun; 179(2):162-8. PubMed ID: 8758208
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
    Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.