96 related articles for article (PubMed ID: 8358433)
1. Telomere capture stabilizes chromosome breakage.
Meltzer PS; Guan XY; Trent JM
Nat Genet; 1993 Jul; 4(3):252-5. PubMed ID: 8358433
[TBL] [Abstract][Full Text] [Related]
2. Frequency of chromosome healing and interstitial telomeres in 40 cases of constitutional abnormalities.
Fortin F; Beaulieu Bergeron M; Fetni R; Lemieux N
Cytogenet Genome Res; 2009; 125(3):176-85. PubMed ID: 19738378
[TBL] [Abstract][Full Text] [Related]
3. FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes.
Ballif BC; Kashork CD; Shaffer LG
Eur J Hum Genet; 2000 Oct; 8(10):764-70. PubMed ID: 11039576
[TBL] [Abstract][Full Text] [Related]
4. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions.
Ballif BC; Yu W; Shaw CA; Kashork CD; Shaffer LG
Hum Mol Genet; 2003 Sep; 12(17):2153-65. PubMed ID: 12915474
[TBL] [Abstract][Full Text] [Related]
5. The loss of a single telomere can result in instability of multiple chromosomes in a human tumor cell line.
Sabatier L; Ricoul M; Pottier G; Murnane JP
Mol Cancer Res; 2005 Mar; 3(3):139-50. PubMed ID: 15798094
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Telomere healing following DNA polymerase arrest-induced breakages is likely the main mechanism generating chromosome 4p terminal deletions.
Hannes F; Van Houdt J; Quarrell OW; Poot M; Hochstenbach R; Fryns JP; Vermeesch JR
Hum Mutat; 2010 Dec; 31(12):1343-51. PubMed ID: 20886614
[TBL] [Abstract][Full Text] [Related]
8. Telomeres and chromosome instability.
Murnane JP
DNA Repair (Amst); 2006 Sep; 5(9-10):1082-92. PubMed ID: 16784900
[TBL] [Abstract][Full Text] [Related]
9. Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies.
Brezinová J; Zemanová Z; Ransdorfová S; Pavlistová L; Babická L; Housková L; Melichercíková J; Sisková M; Cermák J; Michalová K
Cancer Genet Cytogenet; 2007 Feb; 173(1):10-6. PubMed ID: 17284364
[TBL] [Abstract][Full Text] [Related]
10. 13q deletions in B-cell lymphoproliferative disorders: frequent association with translocation.
Struski S; Helias C; Gervais C; Audhuy B; Zamfir A; Herbrecht R; Lessard M
Cancer Genet Cytogenet; 2007 Apr; 174(2):151-60. PubMed ID: 17452258
[TBL] [Abstract][Full Text] [Related]
11. Pathogenesis of jumping translocations: a molecular cytogenetics study.
Wan TS; Ma SK; Chow EY; Li YH; Lin SY; Chan LC
Leuk Res; 2004 Oct; 28(10):1075-9. PubMed ID: 15289020
[TBL] [Abstract][Full Text] [Related]
12. Several chromosomes involved in translocations with chromosome 5 shown with fluorescence in situ hybridization in patients with malignant myeloid disorders.
Bram S; Rödjer S; Swolin B
Cancer Genet Cytogenet; 2004 Nov; 155(1):74-8. PubMed ID: 15527906
[TBL] [Abstract][Full Text] [Related]
13. Diverse chromosome breakage mechanisms underlie subtelomeric rearrangements, a common cause of mental retardation.
Rooms L; Reyniers E; Kooy RF
Hum Mutat; 2007 Feb; 28(2):177-82. PubMed ID: 16991117
[TBL] [Abstract][Full Text] [Related]
14. Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded child.
Lorda-Sanchez I; Lopez-Pajares I; Roche MC; Sanz R; Rodriguez de Alba M; Gonzalez-Gonzalez MC; Ibañez A; Ramos C; Ayuso C
Am J Med Genet; 2000 Dec; 95(4):336-8. PubMed ID: 11186887
[TBL] [Abstract][Full Text] [Related]
15. Chromosome 1 abnormalities in multiple myeloma.
Marzin Y; Jamet D; Douet-Guilbert N; Morel F; Le Bris MJ; Morice P; Abgrall JF; Berthou C; De Braekeleer M
Anticancer Res; 2006; 26(2A):953-9. PubMed ID: 16619492
[TBL] [Abstract][Full Text] [Related]
16. Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH.
Pettenati MJ; Jackle B; Bobby P; Stewart W; Von Kap-Herr C; Mowrey P; Rao PN; May KM
Am J Med Genet; 2002 Jul; 111(1):48-53. PubMed ID: 12124733
[TBL] [Abstract][Full Text] [Related]
17. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
18. Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL.
Brown J; Horsley SW; Jung C; Saracoglu K; Janssen B; Brough M; Daschner M; Beedgen B; Kerkhoffs G; Eils R; Harris PC; Jauch A; Kearney L
Eur J Hum Genet; 2000 Dec; 8(12):903-10. PubMed ID: 11175277
[TBL] [Abstract][Full Text] [Related]
19. A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration.
Nat Genet; 1996 Sep; 14(1):86-9. PubMed ID: 8782825
[TBL] [Abstract][Full Text] [Related]
20. Prenatal exclusion of subtelomeric deletion 1p by fluorescent in situ hybridization.
Phupong V; Praphanphoj V; Shotelersuk V
Arch Gynecol Obstet; 2007 Apr; 275(4):237-40. PubMed ID: 16983561
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
