BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 2168204)

  • 21. [Congenital aniridia and cataract].
    Speeg-Schatz C
    J Fr Ophtalmol; 2012 Apr; 35(4):312. PubMed ID: 22001625
    [No Abstract]   [Full Text] [Related]  

  • 22. 11p13 deletion and reduced RBC catalase in a patient with aniridia, glaucoma and bilateral Wilms' tumor.
    Barletta C; Castello MA; Ferrante E; Mavelli I; Clerico A; Ciriolo MR; Vignetti P
    Tumori; 1985 Apr; 71(2):119-21. PubMed ID: 2988163
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.
    Grundy P; Koufos A; Morgan K; Li FP; Meadows AT; Cavenee WK
    Nature; 1988 Nov; 336(6197):374-6. PubMed ID: 2848199
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Evaluation of chromosome 11p imbalances in aniridia and Wilms tumor patients.
    Busch M; Leube B; Thiel A; Schanze I; Beier M; Royer-Pokora B
    Am J Med Genet A; 2013 May; 161A(5):958-64. PubMed ID: 23494989
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Aniridia-Wilms' tumour syndrome--a case report.
    Vidyasagar MS; Sagar SV; Kumar GR; Rao P
    Indian J Ophthalmol; 1992; 40(4):122-3. PubMed ID: 1338631
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.
    Riccardi VM; Sujansky E; Smith AC; Francke U
    Pediatrics; 1978 Apr; 61(4):604-10. PubMed ID: 208044
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.
    Reeve AE; Sih SA; Raizis AM; Feinberg AP
    Mol Cell Biol; 1989 Apr; 9(4):1799-803. PubMed ID: 2542777
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13.
    Francke U; Holmes LB; Atkins L; Riccardi VM
    Cytogenet Cell Genet; 1979; 24(3):185-92. PubMed ID: 225131
    [TBL] [Abstract][Full Text] [Related]  

  • 29. c-Ha-ras1 is not deleted in aniridia-Wilms' tumour association.
    Huerre C; Despoisse S; Gilgenkrantz S; Lenoir GM; Junien C
    Nature; 1983 Oct 13-19; 305(5935):638-41. PubMed ID: 6312328
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare.
    Royer-Pokora B; Ragg S; Heckl-Ostreicher B; Held M; Loos U; Call K; Glaser T; Housman D; Saunders G; Zabel B
    Genes Chromosomes Cancer; 1991 Mar; 3(2):89-100. PubMed ID: 1648959
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A rare case of an isolated PAX6 mutation, aniridia, and Wilms tumor.
    Lind KT; Cost NG; Zegar K; Kuldanek SA; Enzenauer RW; Schneider KW
    Ophthalmic Genet; 2021 Apr; 42(2):216-217. PubMed ID: 33300417
    [No Abstract]   [Full Text] [Related]  

  • 32. Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.
    Yunis JJ; Ramsay NK
    J Pediatr; 1980 Jun; 96(6):1027-30. PubMed ID: 6246230
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Analysis by array CGH of genomic changes associated with the progression or relapse of Wilms' tumour.
    Natrajan R; Little SE; Sodha N; Reis-Filho JS; Mackay A; Fenwick K; Ashworth A; Perlman EJ; Dome JS; Grundy PE; Pritchard-Jones K; Jones C
    J Pathol; 2007 Jan; 211(1):52-9. PubMed ID: 17103382
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Unbalanced translocation of chromosome 3p in Wilms' tumor.
    Walton JM; Lee CL; Mikhail E; Welch JP; Gillis DA
    J Pediatr Surg; 1992 Oct; 27(10):1311-4. PubMed ID: 1328583
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia.
    Crolla JA; van Heyningen V
    Am J Hum Genet; 2002 Nov; 71(5):1138-49. PubMed ID: 12386836
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Lack of linkage of familial Wilms' tumour to chromosomal band 11p13.
    Huff V; Compton DA; Chao LY; Strong LC; Geiser CF; Saunders GF
    Nature; 1988 Nov; 336(6197):377-8. PubMed ID: 2848200
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination.
    Coppes MJ; Bonetta L; Huang A; Hoban P; Chilton-MacNeill S; Campbell CE; Weksberg R; Yeger H; Reeve AE; Williams BR
    Genes Chromosomes Cancer; 1992 Nov; 5(4):326-34. PubMed ID: 1283321
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chromosome number 11 and Wilms' tumor.
    Slater RM; de Kraker J
    Cancer Genet Cytogenet; 1982 Mar; 5(3):237-45. PubMed ID: 6279277
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Further chromosome studies on Wilms' tumor cells of patients without aniridia.
    Kaneko Y; Kondo K; Rowley JD; Moohr JW; Maurer HS
    Cancer Genet Cytogenet; 1983 Oct; 10(2):191-7. PubMed ID: 6311403
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Inactivation of the remaining allele of the WT1 gene in a Wilms' tumour from a WAGR patient.
    Brown KW; Watson JE; Poirier V; Mott MG; Berry PJ; Maitland NJ
    Oncogene; 1992 Apr; 7(4):763-8. PubMed ID: 1314370
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.