263 related articles for article (PubMed ID: 15968688)
1. Chromosome abnormalities in juxtaglomerular cell tumors.
Brandal P; Busund LT; Heim S
Cancer; 2005 Aug; 104(3):504-10. PubMed ID: 15968688
[TBL] [Abstract][Full Text] [Related]
2. Loss of chromosomes 9 and 11 may be recurrent chromosome imbalances in juxtaglomerular cell tumors.
Capovilla M; Couturier J; Molinié V; Amsellem-Ouazana D; Priollet P; Baumert H; Bruneval P; Vieillefond A
Hum Pathol; 2008 Mar; 39(3):459-62. PubMed ID: 18261631
[TBL] [Abstract][Full Text] [Related]
3. [Juxtaglomerular cell tumors: report of two cases with genomic analysis].
Capovilla M; Couturier J; Molinié V; Bruneval P; Vieillefond A
Ann Pathol; 2008 Oct; 28(5):474-6. PubMed ID: 19068398
[TBL] [Abstract][Full Text] [Related]
4. Juxtaglomerular cell tumor in an 8-year-old girl.
Shao L; Manalang M; Cooley L
Pediatr Blood Cancer; 2008 Feb; 50(2):406-9. PubMed ID: 16972237
[TBL] [Abstract][Full Text] [Related]
5. Numerical chromosome 1, 7, 9, and 11 aberrations in bladder cancer detected by in situ hybridization.
Hopman AH; Moesker O; Smeets AW; Pauwels RP; Vooijs GP; Ramaekers FC
Cancer Res; 1991 Jan; 51(2):644-51. PubMed ID: 1985781
[TBL] [Abstract][Full Text] [Related]
6. Bladder irrigation specimens assayed by fluorescence in situ hybridization to interphase nuclei.
Wheeless LL; Reeder JE; Han R; O'Connell MJ; Frank IN; Cockett AT; Hopman AH
Cytometry; 1994 Dec; 17(4):319-26. PubMed ID: 7875039
[TBL] [Abstract][Full Text] [Related]
7. Molecular genetic evidence for the independent origin of multifocal papillary tumors in patients with papillary renal cell carcinomas.
Jones TD; Eble JN; Wang M; MacLennan GT; Delahunt B; Brunelli M; Martignoni G; Lopez-Beltran A; Bonsib SM; Ulbright TM; Zhang S; Nigro K; Cheng L
Clin Cancer Res; 2005 Oct; 11(20):7226-33. PubMed ID: 16243792
[TBL] [Abstract][Full Text] [Related]
8. Juxtaglomerular cell tumor: a morphological, immunohistochemical and genetic study of six cases.
Kuroda N; Maris S; Monzon FA; Tan PH; Thomas A; Petersson FB; Gatalica Z; Ghazalpour A; Bender RP; Grossmann P; Michal M; Svajdler M; Ovcak Z; Hora M; Hes O
Hum Pathol; 2013 Jan; 44(1):47-54. PubMed ID: 22939575
[TBL] [Abstract][Full Text] [Related]
9. Analysis of ameloblastomas by comparative genomic hybridization and fluorescence in situ hybridization.
Toida M; Balázs M; Treszl A; Rákosy Z; Kato K; Yamazaki Y; Matsui T; Suwa T; Hatakeyama D; Makita H; Mori S; Yamashita T; Shibata T; Adány R
Cancer Genet Cytogenet; 2005 Jun; 159(2):99-104. PubMed ID: 15899380
[TBL] [Abstract][Full Text] [Related]
10. Multipoint interphase FISH in childhood T-acute lymphoblastic leukemia detects subpopulations that carry different chromosome 3 aberrations.
Haltrich I; Kost-Alimova M; Kovács G; Dobos M; Klein G; Fekete G; Imreh S
Cancer Genet Cytogenet; 2007 Jan; 172(1):54-60. PubMed ID: 17175380
[TBL] [Abstract][Full Text] [Related]
11. Chromosome 7 abnormalities are common in chordomas.
Brandal P; Bjerkehagen B; Danielsen H; Heim S
Cancer Genet Cytogenet; 2005 Jul; 160(1):15-21. PubMed ID: 15949565
[TBL] [Abstract][Full Text] [Related]
12. Characteristic pattern of genetic aberrations in ovarian granulosa cell tumors.
Mayr D; Kaltz-Wittmer C; Arbogast S; Amann G; Aust DE; Diebold J
Mod Pathol; 2002 Sep; 15(9):951-7. PubMed ID: 12218213
[TBL] [Abstract][Full Text] [Related]
13. A combination of molecular cytogenetic analyses reveals complex genetic alterations in conventional renal cell carcinoma.
Strefford JC; Stasevich I; Lane TM; Lu YJ; Oliver T; Young BD
Cancer Genet Cytogenet; 2005 May; 159(1):1-9. PubMed ID: 15860350
[TBL] [Abstract][Full Text] [Related]
14. Cytogenetic analyses of premature ovarian failure using karyotyping and interphase fluorescence in situ hybridization (FISH) in a group of 1000 patients.
Lakhal B; Braham R; Berguigua R; Bouali N; Zaouali M; Chaieb M; Veitia RA; Saad A; Elghezal H
Clin Genet; 2010 Aug; 78(2):181-5. PubMed ID: 20345472
[TBL] [Abstract][Full Text] [Related]
15. Incidence of numerical chromosome aberrations in meningioma tumors as revealed by fluorescence in situ hybridization using 10 chromosome-specific probes.
Sayagués JM; Tabernero MD; Maillo A; Díaz P; Rasillo A; Bortoluci A; Gomez-Moreta J; Santos-Briz A; Morales F; Orfao A
Cytometry; 2002 Jun; 50(3):153-9. PubMed ID: 12116338
[TBL] [Abstract][Full Text] [Related]
16. Regional deletion and amplification on chromosome 6 in a uveal melanoma case without abnormalities on chromosomes 1p, 3 and 8.
van Gils W; Kilic E; Brüggenwirth HT; Vaarwater J; Verbiest MM; Beverloo B; van Til-Berg ME; Paridaens D; Luyten GP; de Klein A
Melanoma Res; 2008 Feb; 18(1):10-5. PubMed ID: 18227702
[TBL] [Abstract][Full Text] [Related]
17. Molecular cytogenetic analysis of oral squamous cell carcinomas by comparative genomic hybridization, spectral karyotyping, and fluorescence in situ hybridization.
Uchida K; Oga A; Okafuji M; Mihara M; Kawauchi S; Furuya T; Chochi Y; Ueyama Y; Sasaki K
Cancer Genet Cytogenet; 2006 Jun; 167(2):109-16. PubMed ID: 16737909
[TBL] [Abstract][Full Text] [Related]
18. Molecular cytogenetic analysis of human spermatocytic seminomas.
Verdorfer I; Rogatsch H; Tzankov A; Steiner H; Mikuz G
J Pathol; 2004 Nov; 204(3):277-81. PubMed ID: 15476269
[TBL] [Abstract][Full Text] [Related]
19. Characterization of chromosome 14 abnormalities by interphase in situ hybridization and comparative genomic hybridization in 124 meningiomas: correlation with clinical, histopathologic, and prognostic features.
Tabernero MD; Espinosa AB; Maíllo A; Sayagués JM; Alguero Mdel C; Lumbreras E; Díaz P; Gonçalves JM; Onzain I; Merino M; Morales F; Orfao A
Am J Clin Pathol; 2005 May; 123(5):744-51. PubMed ID: 15981814
[TBL] [Abstract][Full Text] [Related]
20. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
