104 related articles for article (PubMed ID: 22982889)
1. Identification of tissue contamination by polymorphic deletion probe fluorescence in situ hybridization.
Chiang S; Yip S; Betensky RA; Batten JM; Misdraji J; John Iafrate A
Am J Surg Pathol; 2012 Oct; 36(10):1464-71. PubMed ID: 22982889
[TBL] [Abstract][Full Text] [Related]
2. Diagnosis of hydatidiform moles by polymorphic deletion probe fluorescence in situ hybridization.
Chiang S; Fazlollahi L; Nguyen A; Betensky RA; Roberts DJ; Iafrate AJ
J Mol Diagn; 2011 Jul; 13(4):406-15. PubMed ID: 21704275
[TBL] [Abstract][Full Text] [Related]
3. An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
Iourov IY; Soloviev IV; Vorsanova SG; Monakhov VV; Yurov YB
J Histochem Cytochem; 2005 Mar; 53(3):401-8. PubMed ID: 15750029
[TBL] [Abstract][Full Text] [Related]
4. The changing spectrum of DNA-based specimen provenance testing in surgical pathology.
Pfeifer JD; Zehnbauer B; Payton J
Am J Clin Pathol; 2011 Jan; 135(1):132-8. PubMed ID: 21173135
[TBL] [Abstract][Full Text] [Related]
5. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
Ulmer R; Pfeiffer RA; Kollert A; Beinder E
Z Geburtshilfe Neonatol; 2000; 204(1):1-7. PubMed ID: 10721179
[TBL] [Abstract][Full Text] [Related]
6. Sexing of human embryos and fetuses by fluorescent in situ hybridization (FISH) to paraffin-embedded tissues with sex chromosome-specific DNA probes.
Mori C; Shiota K
Am J Med Genet; 1994 Apr; 50(2):180-6. PubMed ID: 8010350
[TBL] [Abstract][Full Text] [Related]
7. Simultaneous detection of multiple genetic aberrations in single cells by spectral fluorescence in situ hybridization.
Slovak ML; Tcheurekdjian L; Zhang FF; Murata-Collins JL
Cancer Res; 2001 Feb; 61(3):831-6. PubMed ID: 11221864
[TBL] [Abstract][Full Text] [Related]
8. Molecular diagnosis of Ewing sarcoma family of tumors: a comparative analysis of 560 cases with FISH and RT-PCR.
Machado I; Noguera R; Pellin A; Lopez-Guerrero JA; Piqueras M; Navarro S; Llombart-Bosch A
Diagn Mol Pathol; 2009 Dec; 18(4):189-99. PubMed ID: 19861898
[TBL] [Abstract][Full Text] [Related]
9. Direct detection of fetal cells in maternal blood: a reappraisal using a combination of two different Y chromosome-specific FISH probes and a single X chromosome-specific probe.
Babochkina T; Mergenthaler S; Dinges TM; Holzgreve W; Hahn S
Arch Gynecol Obstet; 2005 Dec; 273(3):166-9. PubMed ID: 16133462
[TBL] [Abstract][Full Text] [Related]
10. Rate of occult specimen provenance complications in routine clinical practice.
Pfeifer JD; Liu J
Am J Clin Pathol; 2013 Jan; 139(1):93-100. PubMed ID: 23270904
[TBL] [Abstract][Full Text] [Related]
11. Fluorescent in situ hybridization (FISH) on paraffin-embedded placental tissues as an adjunct for understanding the etiology of early spontaneous abortion.
Lescoat D; Jouan H; Loeuillet-Olivo L; Le Calvé M
Prenat Diagn; 2005 Apr; 25(4):314-7. PubMed ID: 15849799
[TBL] [Abstract][Full Text] [Related]
12. Extraneous tissue: a potential source for diagnostic error in surgical pathology.
Layfield LJ; Witt BL; Metzger KG; Anderson GM
Am J Clin Pathol; 2011 Nov; 136(5):767-72. PubMed ID: 22031316
[TBL] [Abstract][Full Text] [Related]
13. Enhanced detection of spitzoid melanomas using fluorescence in situ hybridization with 9p21 as an adjunctive probe.
Gammon B; Beilfuss B; Guitart J; Gerami P
Am J Surg Pathol; 2012 Jan; 36(1):81-8. PubMed ID: 21989344
[TBL] [Abstract][Full Text] [Related]
14. Fluorescence in situ hybridization method in isolated single nuclei extracted from paraffin-embedded hepatocellular carcinoma tissues.
Tantiwetrueangdet A; Panvichian R; Sornmayura P; Pinpradap K; Leelaudomlipi S
J Med Assoc Thai; 2007 Feb; 90(2):363-8. PubMed ID: 17375644
[TBL] [Abstract][Full Text] [Related]
15. Quantitative analysis of chimerism after allogeneic stem cell transplantation by real-time polymerase chain reaction with single nucleotide polymorphisms, standard tandem repeats, and Y-chromosome-specific sequences.
Koldehoff M; Steckel NK; Hlinka M; Beelen DW; Elmaagacli AH
Am J Hematol; 2006 Oct; 81(10):735-46. PubMed ID: 16838323
[TBL] [Abstract][Full Text] [Related]
16. Identification of sex chromosome by fluorescence in situ hybridization.
Sarasophona S; Promsawat K; Rerkamnuaychok B
J Med Assoc Thai; 2000 Mar; 83 Suppl 1():S89-94. PubMed ID: 10865413
[TBL] [Abstract][Full Text] [Related]
17. Sensitive detection of chromosome copy number aberrations in prostate cancer by fluorescence in situ hybridization.
Visakorpi T; Hyytinen E; Kallioniemi A; Isola J; Kallioniemi OP
Am J Pathol; 1994 Sep; 145(3):624-30. PubMed ID: 8080044
[TBL] [Abstract][Full Text] [Related]
18. Numerical abnormalities of chromosome 7 in human prostate cancer detected by fluorescence in situ hybridization (FISH) on paraffin-embedded tissue sections with centromere-specific DNA probes.
Zitzelsberger H; Szücs S; Weier HU; Lehmann L; Braselmann H; Enders S; Schilling A; Breul J; Höfler H; Bauchinger M
J Pathol; 1994 Apr; 172(4):325-35. PubMed ID: 8207613
[TBL] [Abstract][Full Text] [Related]
19. Detection of Y chromosome sequences in a 45,X/46,XXq--patient by Southern blot analysis of PCR-amplified DNA and fluorescent in situ hybridization (FISH).
Kocova M; Siegel SF; Wenger SL; Lee PA; Nalesnik M; Trucco M
Am J Med Genet; 1995 Feb; 55(4):483-8. PubMed ID: 7762591
[TBL] [Abstract][Full Text] [Related]
20. The challenge and importance of standardizing pre-analytical variables in surgical pathology specimens for clinical care and translational research.
Hicks DG; Boyce BF
Biotech Histochem; 2012 Jan; 87(1):14-7. PubMed ID: 21732745
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]