267 related articles for article (PubMed ID: 17311249)
1. DNA sequence of the translocation breakpoints in undifferentiated embryonal sarcoma arising in mesenchymal hamartoma of the liver harboring the t(11;19)(q11;q13.4) translocation.
Rajaram V; Knezevich S; Bove KE; Perry A; Pfeifer JD
Genes Chromosomes Cancer; 2007 May; 46(5):508-13. PubMed ID: 17311249
[TBL] [Abstract][Full Text] [Related]
2. Characterization of translocations in mesenchymal hamartoma and undifferentiated embryonal sarcoma of the liver.
Mathews J; Duncavage EJ; Pfeifer JD
Exp Mol Pathol; 2013 Dec; 95(3):319-24. PubMed ID: 24120702
[TBL] [Abstract][Full Text] [Related]
3. Hepatic mesenchymal hamartoma with translocation involving chromosome band 19q13.4: a recurrent abnormality.
Rakheja D; Margraf LR; Tomlinson GE; Schneider NR
Cancer Genet Cytogenet; 2004 Aug; 153(1):60-3. PubMed ID: 15325096
[TBL] [Abstract][Full Text] [Related]
4. Undifferentiated embryonal sarcoma with unusual features arising within mesenchymal hamartoma of the liver: report of a case and review of the literature.
O'Sullivan MJ; Swanson PE; Knoll J; Taboada EM; Dehner LP
Pediatr Dev Pathol; 2001; 4(5):482-9. PubMed ID: 11779051
[TBL] [Abstract][Full Text] [Related]
5. Third report of t(19q)(13.4) in mesenchymal hamartoma of liver with comments on link to embryonal sarcoma.
Bove KE; Blough RI; Soukup S
Pediatr Dev Pathol; 1998; 1(5):438-42. PubMed ID: 9688769
[TBL] [Abstract][Full Text] [Related]
6. Undifferentiated embryonal sarcoma of the liver is associated with mesenchymal hamartoma and multiple chromosomal abnormalities: a review of eleven cases.
Shehata BM; Gupta NA; Katzenstein HM; Steelman CK; Wulkan ML; Gow KW; Bridge JA; Kenney BD; Thompson K; de Chadarévian JP; Abramowsky CR
Pediatr Dev Pathol; 2011; 14(2):111-6. PubMed ID: 20925497
[TBL] [Abstract][Full Text] [Related]
7. Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases.
Hearle N; Lucassen A; Wang R; Lim W; Ross F; Wheeler R; Moore I; Shipley J; Houlston R
Genes Chromosomes Cancer; 2004 Oct; 41(2):163-9. PubMed ID: 15287029
[TBL] [Abstract][Full Text] [Related]
8. A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9.
Boyadjiev SA; South ST; Radford CL; Patel A; Zhang G; Hur DJ; Thomas GH; Gearhart JP; Stetten G
Genomics; 2005 May; 85(5):622-9. PubMed ID: 15820314
[TBL] [Abstract][Full Text] [Related]
9. PVRL2 is translocated to the TRA@ locus in t(14;19)(q11;q13)-positive peripheral T-cell lymphomas.
Almire C; Bertrand P; Ruminy P; Maingonnat C; Wlodarska I; Martín-Subero JI; Siebert R; Tilly H; Bastard C
Genes Chromosomes Cancer; 2007 Nov; 46(11):1011-8. PubMed ID: 17696193
[TBL] [Abstract][Full Text] [Related]
10. Mesenchymal hamartoma of the liver with inversion of chromosome 19.
Shetty S; Pinto A; Roland B
Pediatr Dev Pathol; 2011; 14(5):407-10. PubMed ID: 21426235
[TBL] [Abstract][Full Text] [Related]
11. Undifferentiated (embryonal) sarcoma arising in conjunction with mesenchymal hamartoma of the liver.
de Chadarévian JP; Pawel BR; Faerber EN; Weintraub WH
Mod Pathol; 1994 May; 7(4):490-3. PubMed ID: 8066077
[TBL] [Abstract][Full Text] [Related]
12. Characterization of t(6;11)(p21;q12) in a renal-cell carcinoma of an adult patient.
Pecciarini L; Cangi MG; Lo Cunsolo C; Macri' E; Dal Cin E; Martignoni G; Doglioni C
Genes Chromosomes Cancer; 2007 May; 46(5):419-26. PubMed ID: 17285572
[TBL] [Abstract][Full Text] [Related]
13. Myxoid liposarcoma with t(12;16) (q13;p11) contains site-specific differences in methylation patterns surrounding a zinc-finger gene mapped to the breakpoint region on chromosome 12.
Paulien S; Turc-Carel C; Dal Cin P; Jani-Sait S; Sreekantaiah C; Leong SP; Vogelstein B; Kinzler KW; Sandberg AA; Gemmill RM
Cancer Res; 1990 Dec; 50(24):7902-7. PubMed ID: 2253229
[TBL] [Abstract][Full Text] [Related]
14. A KRAB zinc finger protein gene is the potential target of 19q13 translocation in benign thyroid tumors.
Rippe V; Belge G; Meiboom M; Kazmierczak B; Fusco A; Bullerdiek J
Genes Chromosomes Cancer; 1999 Nov; 26(3):229-36. PubMed ID: 10502321
[TBL] [Abstract][Full Text] [Related]
15. Second report of a translocation involving 19q13.4 in a mesenchymal hamartoma of the liver.
Mascarello JT; Krous HF
Cancer Genet Cytogenet; 1992 Feb; 58(2):141-2. PubMed ID: 1551077
[TBL] [Abstract][Full Text] [Related]
16. Recurrent mesenchymal hamartoma associated with 19q translocation. A call for more radical surgical resection.
Sharif K; Ramani P; Lochbühler H; Grundy R; de Ville de Goyet J
Eur J Pediatr Surg; 2006 Feb; 16(1):64-7. PubMed ID: 16544232
[TBL] [Abstract][Full Text] [Related]
17. A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation.
McMullan TW; Crolla JA; Gregory SG; Carter NP; Cooper RA; Howell GR; Robinson DO
Hum Genet; 2002 Mar; 110(3):244-50. PubMed ID: 11935336
[TBL] [Abstract][Full Text] [Related]
18. A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).
Nimmakayalu MA; Gotter AL; Shaikh TH; Emanuel BS
Hum Mol Genet; 2003 Nov; 12(21):2817-25. PubMed ID: 12952865
[TBL] [Abstract][Full Text] [Related]
19. Mesenchymal hamartoma of the liver originating in the caudate lobe with t(11;19)(q13;q13.4): report of a case.
Sugito K; Kawashima H; Uekusa S; Inoue M; Ikeda T; Kusafuka T
Surg Today; 2010; 40(1):83-7. PubMed ID: 20037848
[TBL] [Abstract][Full Text] [Related]
20. The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome.
Duba HC; Doll A; Neyer M; Erdel M; Mann C; Hammerer I; Utermann G; Grzeschik KH
Eur J Hum Genet; 2002 Jun; 10(6):351-61. PubMed ID: 12080386
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]