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.
421 related articles for article (PubMed ID: 8082483)
1. Cytogenetic analysis by chromosome painting. Carter NP Cytometry; 1994 Mar; 18(1):2-10. PubMed ID: 8082483 [TBL] [Abstract][Full Text] [Related]
2. Paint-assisted microdissection-FISH: Rapid and simple mapping of translocation breakpoints in the embryonal rhabdomyosarcoma cell line RD. Roberts I; Foster N; Nacheva E; Coleman N Cytometry A; 2004 Apr; 58(2):177-84. PubMed ID: 15057971 [TBL] [Abstract][Full Text] [Related]
3. Spectral karyotyping analysis of head and neck squamous cell carcinoma. Singh B; Gogineni S; Goberdhan A; Sacks P; Shaha A; Shah J; Rao P Laryngoscope; 2001 Sep; 111(9):1545-50. PubMed ID: 11568603 [TBL] [Abstract][Full Text] [Related]
4. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting]. Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073 [TBL] [Abstract][Full Text] [Related]
5. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping. Veldman T; Vignon C; Schröck E; Rowley JD; Ried T Nat Genet; 1997 Apr; 15(4):406-10. PubMed ID: 9090389 [TBL] [Abstract][Full Text] [Related]
7. Genetic analysis by chromosome sorting and painting: phylogenetic and diagnostic applications. Ferguson-Smith MA Eur J Hum Genet; 1997; 5(5):253-65. PubMed ID: 9412781 [TBL] [Abstract][Full Text] [Related]
8. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Speicher MR; Gwyn Ballard S; Ward DC Nat Genet; 1996 Apr; 12(4):368-75. PubMed ID: 8630489 [TBL] [Abstract][Full Text] [Related]
9. A classification efficiency test of spectral karyotyping and multiplex fluorescence in situ hybridization: identification of chromosome homologies between Homo sapiens and Hylobates leucogenys. Rens W; Yang F; O'Brien PC; Solanky N; Ferguson-Smith MA Genes Chromosomes Cancer; 2001 May; 31(1):65-74. PubMed ID: 11284037 [TBL] [Abstract][Full Text] [Related]
10. Use of chromosome painting for marker chromosome identification in two children with congenital disorders. Doco-Fenzy M; Navrocki B; Cornillet P; Sabouraud P; Robillard P; Gruson N; Gaillard D; Adnet JJ Bull Assoc Anat (Nancy); 1994 Jun; 78(241):9-13. PubMed ID: 8086666 [TBL] [Abstract][Full Text] [Related]
11. [Cytogenetic study of 121 patients suffering from various hematologic neoplasms using the in situ hybridization technique]. Pérez Losada A; Solé F; Woessner S; Florensa L; Besses C; Espinet B; Caballín MR; García Eroles L; Sans-Sabrafén J Sangre (Barc); 1996 Jun; 41(3):201-9. PubMed ID: 8755208 [TBL] [Abstract][Full Text] [Related]
12. Generation of FISH probes using laser microbeam microdissection and application to clinical molecular cytogenetics. Shim SH; Kyhm JH; Chung SR; Kim SR; Park MI; Lee CH; Cho YH J Microbiol Biotechnol; 2007 Jul; 17(7):1079-82. PubMed ID: 18051316 [TBL] [Abstract][Full Text] [Related]
13. Premature ovarian failure in a patient with a complex chromosome rearrangement involving the critical region Xq24, characterized by analysis using fluorescence in situ hybridization by chromosome microdissection. Weimer J; Shivakumar S; Danda S; Thomas N; Ralui LP; Jonat W; Arnold N Fertil Steril; 2007 Dec; 88(6):1677.e9-13. PubMed ID: 17482166 [TBL] [Abstract][Full Text] [Related]
14. Small marker chromosome identification in metaphase and interphase using centromeric multiplex fish (CM-FISH). Henegariu O; Bray-Ward P; Artan S; Vance GH; Qumsyieh M; Ward DC Lab Invest; 2001 Apr; 81(4):475-81. PubMed ID: 11304566 [TBL] [Abstract][Full Text] [Related]
15. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting. Coêlho KE; Egashira M; Kato R; Fujimoto M; Matsumoto N; Rerkamnuaychoke B; Abe K; Harada N; Ohashi H; Fukushima Y; Niikawa N Am J Med Genet; 1996 Jun; 63(3):468-71. PubMed ID: 8737654 [TBL] [Abstract][Full Text] [Related]
16. Karyotyping lymph node biopsies in non-Hodgkin's lymphoma. Ross FM; Harrison CJ Methods Mol Med; 2005; 115():93-107. PubMed ID: 15998964 [TBL] [Abstract][Full Text] [Related]
17. [Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics]. Douet-Guilbert N; Basinko A; Le Bris MJ; Herry A; Morel F; De Braekeleer M Pathol Biol (Paris); 2008 Sep; 56(6):362-7. PubMed ID: 18456432 [TBL] [Abstract][Full Text] [Related]
18. Identification and fate of a marker chromosome in methotrexate-resistant V79,B7 cells by flow karyotyping and sorting, metaphase analysis and in situ hybridization. Nüsse M; Viaggi S; Bonatti S Anal Cell Pathol; 1992 Sep; 4(5):345-58. PubMed ID: 1445793 [TBL] [Abstract][Full Text] [Related]
19. Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY). Cohen N; Betts DR; Trakhtenbrot L; Niggli FK; Amariglio N; Brok-Simoni F; Rechavi G; Meitar D Genes Chromosomes Cancer; 2001 Jul; 31(3):201-8. PubMed ID: 11391790 [TBL] [Abstract][Full Text] [Related]