These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
98 related articles for article (PubMed ID: 8258302)
1. Intragenic reorganization of RB1 in a complex (4;13) rearrangement demonstrated by FISH. Rosenberg C; Janson M; Nordeskjöld M; Børresen AL; Vianna-Morgante AM Cytogenet Cell Genet; 1994; 65(4):268-71. PubMed ID: 8258302 [TBL] [Abstract][Full Text] [Related]
2. Detection of retinoblastoma gene copy number in metaphase chromosomes and interphase nuclei by fluorescence in situ hybridization. Kallioniemi A; Kallioniemi OP; Waldman FM; Chen LC; Yu LC; Fung YK; Smith HS; Pinkel D; Gray JW Cytogenet Cell Genet; 1992; 60(3-4):190-3. PubMed ID: 1354594 [TBL] [Abstract][Full Text] [Related]
3. De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: report and review. Batanian JR; Eswara MS Am J Med Genet; 1998 Jun; 78(1):44-51. PubMed ID: 9637422 [TBL] [Abstract][Full Text] [Related]
4. Characterization by FISH of a t(5;13) in a patient with bilateral retinoblastoma. Triviño E; Guitart M; Egozcue J; Coll MD Cancer Genet Cytogenet; 1997 Jul; 96(1):23-5. PubMed ID: 9209465 [TBL] [Abstract][Full Text] [Related]
5. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia. Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352 [TBL] [Abstract][Full Text] [Related]
6. De novo double reciprocal translocations in addition to partial monosomy at another chromosome: A very rare case. Simioni M; Steiner CE; Gil-da-Silva-Lopes VL Gene; 2015 Nov; 573(1):166-70. PubMed ID: 26318482 [TBL] [Abstract][Full Text] [Related]
7. De novo complex chromosome rearrangement: a study of two patients. Melo DG; Huber J; Giuliani LR; Mazzucatto LF; Riegel M; Pina-Neto JM Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822 [TBL] [Abstract][Full Text] [Related]
8. Molecular cytogenetic characterization of 17 rob(13q14q) Robertsonian translocations by FISH, narrowing the region containing the breakpoints. Han JY; Choo KH; Shaffer LG Am J Hum Genet; 1994 Nov; 55(5):960-7. PubMed ID: 7977359 [TBL] [Abstract][Full Text] [Related]
9. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping. Peschka B; Leygraaf J; Hansmann D; Hansmann M; Schröck E; Ried T; Engels H; Schwanitz G; Schubert R Prenat Diagn; 1999 Dec; 19(12):1143-9. PubMed ID: 10590433 [TBL] [Abstract][Full Text] [Related]
10. Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization. Sullivan BA; Leana-Cox J; Schwartz S Am J Med Genet; 1993 Aug; 47(2):223-30. PubMed ID: 8213910 [TBL] [Abstract][Full Text] [Related]
11. Primed in situ labeling (PRINS) for evaluation of gene deletions in cancer. Tharapel SA; Kadandale JS Am J Med Genet; 2002 Jan; 107(2):123-6. PubMed ID: 11807886 [TBL] [Abstract][Full Text] [Related]
12. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma]. Laureys GG Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670 [TBL] [Abstract][Full Text] [Related]
13. Retinoblastoma and deletion of the long arm of chromosome 13: an underestimated diagnosis? Brichard B; Chantrain C; Gala JL; Sibille C; Vermylen C; De Potter P Pediatr Blood Cancer; 2008 Mar; 50(3):694-6. PubMed ID: 16856159 [TBL] [Abstract][Full Text] [Related]
14. Centromeric alpha-satellite DNA break in reciprocal translocations. Wang JC; Hajianpour A; Habibian R Cytogenet Genome Res; 2009; 125(4):329-33. PubMed ID: 19864896 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. De novo balanced complex chromosome rearrangement (CCR) involving chromosome 8, 11 and 16 in a boy with mild developmental delay and psychotic disorder. Goumy C; Mihaescu M; Tchirkov A; Giollant M; Benier C; Francannet C; Jaffray JY; Geneix A; Vago P Genet Couns; 2006; 17(3):371-9. PubMed ID: 17100206 [TBL] [Abstract][Full Text] [Related]
17. Chromosomal assignment of retinoblastoma 1 gene (RB1) to mouse 14D3 and rat 15q12 by fluorescence in situ hybridization. Ono T; Yoshida MC Jpn J Genet; 1993 Dec; 68(6):617-21. PubMed ID: 8031579 [TBL] [Abstract][Full Text] [Related]
18. Cytogenetic and molecular investigation of a balanced Xq13q translocation in a patient with retinoblastoma. Stambolian D; Sellinger B; Derrington D; Sargent R; Emanuel BS Am J Med Genet; 1992 Apr; 42(6):771-6. PubMed ID: 1554012 [TBL] [Abstract][Full Text] [Related]
19. [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ]. Balícek P; Jüttnerová V; Jarosová M; Fialová J; Fiedler Z; Kolmanová J Cas Lek Cesk; 2001 Mar; 140(4):122-4. PubMed ID: 11284430 [TBL] [Abstract][Full Text] [Related]
20. Complete association of loss of heterozygosity of chromosomes 13 and 17 in osteosarcoma. Scheffer H; Kruize YC; Osinga J; Kuiken G; Oosterhuis JW; Leeuw JA; Schraffordt Koops H; Buys CH Cancer Genet Cytogenet; 1991 May; 53(1):45-55. PubMed ID: 2036639 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]