166 related articles for article (PubMed ID: 9679749)
1. Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome.
Miozzo M; Castorina P; Riva P; Dalprà L; Fuhrman Conti AM; Volpi L; Hoe TS; Khoo A; Wiegant J; Rosenberg C; Larizza L
Int J Cancer; 1998 Aug; 77(4):504-10. PubMed ID: 9679749
[TBL] [Abstract][Full Text] [Related]
2. Rothmund-Thomson syndrome in siblings: evidence for acquired in vivo mosaicism.
Lindor NM; Devries EM; Michels VV; Schad CR; Jalal SM; Donovan KM; Smithson WA; Kvols LK; Thibodeau SN; Dewald GW
Clin Genet; 1996 Mar; 49(3):124-9. PubMed ID: 8737976
[TBL] [Abstract][Full Text] [Related]
3. Two primary osteosarcomas in a patient with Rothmund-Thomson syndrome.
Anbari KK; Ierardi-Curto LA; Silber JS; Asada N; Spinner N; Zackai EH; Belasco J; Morrissette JD; Dormans JP
Clin Orthop Relat Res; 2000 Sep; (378):213-23. PubMed ID: 10986997
[TBL] [Abstract][Full Text] [Related]
4. Comparative genomic hybridization analysis identifies gains of 1p35 approximately p36 and chromosome 19 in osteosarcoma.
Zielenska M; Bayani J; Pandita A; Toledo S; Marrano P; Andrade J; Petrilli A; Thorner P; Sorensen P; Squire JA
Cancer Genet Cytogenet; 2001 Oct; 130(1):14-21. PubMed ID: 11672768
[TBL] [Abstract][Full Text] [Related]
5. Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas.
Bayani J; Zielenska M; Pandita A; Al-Romaih K; Karaskova J; Harrison K; Bridge JA; Sorensen P; Thorner P; Squire JA
Genes Chromosomes Cancer; 2003 Jan; 36(1):7-16. PubMed ID: 12461745
[TBL] [Abstract][Full Text] [Related]
6. Chromosomal regions involved in the pathogenesis of osteosarcomas.
Stock C; Kager L; Fink FM; Gadner H; Ambros PF
Genes Chromosomes Cancer; 2000 Jul; 28(3):329-36. PubMed ID: 10862039
[TBL] [Abstract][Full Text] [Related]
7. Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH.
Selvarajah S; Yoshimoto M; Ludkovski O; Park PC; Bayani J; Thorner P; Maire G; Squire JA; Zielenska M
Cytogenet Genome Res; 2008; 122(1):5-15. PubMed ID: 18931480
[TBL] [Abstract][Full Text] [Related]
8. Characterization of large chromosome markers in a malignant fibrous histiocytoma by spectral karyotyping, comparative genomic hybridization (CGH), and array CGH.
Weng WH; Wejde J; Ahlén J; Pang ST; Lui WO; Larsson C
Cancer Genet Cytogenet; 2004 Apr; 150(1):27-32. PubMed ID: 15041220
[TBL] [Abstract][Full Text] [Related]
9. Instability of lymphocyte chromosomes in a girl with Rothmund-Thomson syndrome.
Orstavik KH; McFadden N; Hagelsteen J; Ormerod E; van der Hagen CB
J Med Genet; 1994 Jul; 31(7):570-2. PubMed ID: 7966195
[TBL] [Abstract][Full Text] [Related]
10. Cytogenetic findings in a primary malignant fibrous histiocytoma of bone and the lung metastasis.
Bridge JA; Sanger WG; Neff JR; Hess MM
Pathology; 1990 Jan; 22(1):16-9. PubMed ID: 2163505
[TBL] [Abstract][Full Text] [Related]
11. High-resolution mapping of amplifications and deletions in pediatric osteosarcoma by use of CGH analysis of cDNA microarrays.
Squire JA; Pei J; Marrano P; Beheshti B; Bayani J; Lim G; Moldovan L; Zielenska M
Genes Chromosomes Cancer; 2003 Nov; 38(3):215-25. PubMed ID: 14506695
[TBL] [Abstract][Full Text] [Related]
12. Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients.
Wang LL; Levy ML; Lewis RA; Chintagumpala MM; Lev D; Rogers M; Plon SE
Am J Med Genet; 2001 Jul; 102(1):11-7. PubMed ID: 11471165
[TBL] [Abstract][Full Text] [Related]
13. An unusual mutation in RECQ4 gene leading to Rothmund-Thomson syndrome.
Balraj P; Concannon P; Jamal R; Beghini A; Hoe TS; Khoo AS; Volpi L
Mutat Res; 2002 Oct; 508(1-2):99-105. PubMed ID: 12379465
[TBL] [Abstract][Full Text] [Related]
14. Aberrations of chromosomes 1 and 17 in six human osteosarcoma cell lines using double-target fluorescence in situ hybridization.
Murata H; Kusuzaki K; Takeshita H; Hirasawa Y; Ashihara T; Abe T; Inazawa J
Cancer Genet Cytogenet; 1998 Nov; 107(1):7-10. PubMed ID: 9809027
[TBL] [Abstract][Full Text] [Related]
15. [Rothmund-Thomson syndrome, trisomy 8 mosaicism and RECQ4 gene mutation].
Durand F; Castorina P; Morant C; Delobel B; Barouk E; Modiano P
Ann Dermatol Venereol; 2002; 129(6-7):892-5. PubMed ID: 12218919
[TBL] [Abstract][Full Text] [Related]
16. Acquisition of secondary structural chromosomal changes in pediatric ewing sarcoma is a probable prognostic factor for tumor response and clinical outcome.
Zielenska M; Zhang ZM; Ng K; Marrano P; Bayani J; Ramirez OC; Sorensen P; Thorner P; Greenberg M; Squire JA
Cancer; 2001 Jun; 91(11):2156-64. PubMed ID: 11391597
[TBL] [Abstract][Full Text] [Related]
17. Cytogenetic and spectral karyotype analyses of benign and malignant cartilage tumours.
Sjögren H; Orndal C; Tingby O; Meis-Kindblom JM; Kindblom LG; Stenman G
Int J Oncol; 2004 Jun; 24(6):1385-91. PubMed ID: 15138578
[TBL] [Abstract][Full Text] [Related]
18. Rothmund-Thomson syndrome in fraternal twins.
Tong M
Pediatr Dermatol; 1995 Jun; 12(2):134-7. PubMed ID: 7659639
[TBL] [Abstract][Full Text] [Related]
19. Clonal lines of aneuploid cells in Rothmund-Thomson syndrome.
Der Kaloustian VM; McGill JJ; Vekemans M; Kopelman HR
Am J Med Genet; 1990 Nov; 37(3):336-9. PubMed ID: 2260560
[TBL] [Abstract][Full Text] [Related]
20. Evaluation of paediatric osteosarcomas by classic cytogenetic and CGH analyses.
Batanian JR; Cavalli LR; Aldosari NM; Ma E; Sotelo-Avila C; Ramos MB; Rone JD; Thorpe CM; Haddad BR
Mol Pathol; 2002 Dec; 55(6):389-93. PubMed ID: 12456778
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]