122 related articles for article (PubMed ID: 23010713)
1. Array-based karyotyping in plasma cell neoplasia after plasma cell enrichment increases detection of genomic aberrations.
Zehentner BK; Hartmann L; Johnson KR; Stephenson CF; Chapman DB; de Baca ME; Wells DA; Loken MR; Tirtorahardjo B; Gunn SR; Lim L
Am J Clin Pathol; 2012 Oct; 138(4):579-89. PubMed ID: 23010713
[TBL] [Abstract][Full Text] [Related]
2. Risk stratification of plasma cell neoplasm: insights from plasma cell-specific cytoplasmic immunoglobulin fluorescence in situ hybridization (cIg FISH) vs. conventional FISH.
Dong H; Yang HS; Jagannath S; Stephenson CF; Brenholz P; Mazumder A; Chari A
Clin Lymphoma Myeloma Leuk; 2012 Oct; 12(5):366-74. PubMed ID: 22658896
[TBL] [Abstract][Full Text] [Related]
3. High detection rate of clinically relevant genomic abnormalities in plasma cells enriched from patients with multiple myeloma.
Stevens-Kroef M; Weghuis DO; Croockewit S; Derksen L; Hooijer J; Elidrissi-Zaynoun N; Siepman A; Simons A; Kessel AG
Genes Chromosomes Cancer; 2012 Nov; 51(11):997-1006. PubMed ID: 22833442
[TBL] [Abstract][Full Text] [Related]
4. Detection of genomic abnormalities in multiple myeloma: the application of FISH analysis in combination with various plasma cell enrichment techniques.
Hartmann L; Biggerstaff JS; Chapman DB; Scott JM; Johnson KR; Ghirardelli KM; Fritschle WK; Martinez DL; Bennington RK; de Baca ME; Wells DA; Loken MR; Zehentner BK
Am J Clin Pathol; 2011 Nov; 136(5):712-20. PubMed ID: 22031309
[TBL] [Abstract][Full Text] [Related]
5. Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization.
Naus NC; van Drunen E; de Klein A; Luyten GP; Paridaens DA; Alers JC; Ksander BR; Beverloo HB; Slater RM
Genes Chromosomes Cancer; 2001 Mar; 30(3):267-73. PubMed ID: 11170284
[TBL] [Abstract][Full Text] [Related]
6. Integration of conventional cytogenetics, comparative genomic hybridisation and interphase fluorescence in situ hybridisation for the detection of genomic rearrangements in acute leukaemia.
McGrattan P; Campbell S; Cuthbert R; Jones FG; McMullin MF; Humphreys M
J Clin Pathol; 2008 Aug; 61(8):903-8. PubMed ID: 18474541
[TBL] [Abstract][Full Text] [Related]
7. Bacterial artificial chromosome array-based comparative genomic hybridization using paired formalin-fixed, paraffin-embedded and fresh frozen tissue specimens in multiple myeloma.
Lennon PA; Zhuang Y; Pierson D; Zhang X; Williams C; Perez C; Lin P
Cancer; 2009 Jan; 115(2):345-54. PubMed ID: 19109814
[TBL] [Abstract][Full Text] [Related]
8. Comparison of array comparative genomic hybridization (aCGH) to FISH and cytogenetics in prognostic evaluation of chronic lymphocytic leukemia.
O'Malley DP; Giudice C; Chang AS; Chang D; Barry TS; Hibbard MK; Chen R; Chen ST
Int J Lab Hematol; 2011 Jun; 33(3):238-44. PubMed ID: 21143592
[TBL] [Abstract][Full Text] [Related]
9. Applications of array comparative genomic hybridization in obstetrics.
Fruhman G; Van den Veyver IB
Obstet Gynecol Clin North Am; 2010 Mar; 37(1):71-85, Table of Contents. PubMed ID: 20494259
[TBL] [Abstract][Full Text] [Related]
10. Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation.
Gekas J; Vallée M; Castonguay L; Laframboise R; Maranda B; Piedboeuf B; Rousseau F
J Med Genet; 2011 Dec; 48(12):851-5. PubMed ID: 21965346
[TBL] [Abstract][Full Text] [Related]
11. Implementation of cytogenomic microarray with plasma cell enrichment enables better abnormality detection and risk stratification in patients with plasma cell neoplasia than conventional cytogenetics and fluorescence in situ hybridization.
Chen C; Lim AST; Lau LC; Lim TH; Heng EYH; Tien SL
Cancer Genet; 2021 Apr; 252-253():25-36. PubMed ID: 33341677
[TBL] [Abstract][Full Text] [Related]
12. Interphase fluorescence in situ hybridization in multiple myeloma and monoclonal gammopathy of undetermined significance without and with positive plasma cell identification: analysis of 192 cases from the Region of Southern Denmark.
Christensen JH; Abildgaard N; Plesner T; Nibe A; Nielsen O; Sørensen AG; Kerndrup GB;
Cancer Genet Cytogenet; 2007 Apr; 174(2):89-99. PubMed ID: 17452249
[TBL] [Abstract][Full Text] [Related]
13. Interphase fluorescence in situ hybridization on selected plasma cells is superior in the detection of cytogenetic aberrations in plasma cell dyscrasia.
Put N; Lemmens H; Wlodarska I; Konings P; Moreau Y; Hagemeijer A; Vandenberghe P; Michaux L
Genes Chromosomes Cancer; 2010 Nov; 49(11):991-7. PubMed ID: 20662075
[TBL] [Abstract][Full Text] [Related]
14. Molecular cytogenetic aberrations in Tunisian patients with multiple myeloma identified by cIg-FISH in fixed bone marrow cells.
Gmidène A; Avet-Loiseau H; Sennana H; Ben Abdallah I; Khlif A; Meddeb B; Elloumi M; Saad A
Cytogenet Genome Res; 2012; 136(1):44-9. PubMed ID: 22188899
[TBL] [Abstract][Full Text] [Related]
15. Genomic alterations of chromosome region 11p as predictive marker by array comparative genomic hybridization in lung adenocarcinoma patients.
Sung JS; Park KH; Kim YH
Cancer Genet Cytogenet; 2010 Apr; 198(1):27-34. PubMed ID: 20303011
[TBL] [Abstract][Full Text] [Related]
16. Array comparative genomic hybridization of peripheral blood granulocytes of patients with myelodysplastic syndrome detects karyotypic abnormalities.
Vercauteren SM; Sung S; Starczynowski DT; Lam WL; Bruyere H; Horsman DE; Tsang P; Leitch H; Karsan A
Am J Clin Pathol; 2010 Jul; 134(1):119-26. PubMed ID: 20551276
[TBL] [Abstract][Full Text] [Related]
17. Targeting plasma cells improves detection of cytogenetic aberrations in multiple myeloma: phenotype/genotype fluorescence in situ hybridization.
Slovak ML; Bedell V; Pagel K; Chang KL; Smith D; Somlo G
Cancer Genet Cytogenet; 2005 Apr; 158(2):99-109. PubMed ID: 15796956
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array CGH.
Evers C; Beier M; Poelitz A; Hildebrandt B; Servan K; Drechsler M; Germing U; Royer HD; Royer-Pokora B
Genes Chromosomes Cancer; 2007 Dec; 46(12):1119-28. PubMed ID: 17823930
[TBL] [Abstract][Full Text] [Related]
20. The advantage of using SNP array in clinical testing for hematological malignancies--a comparative study of three genetic testing methods.
Xu X; Johnson EB; Leverton L; Arthur A; Watson Q; Chang FL; Raca G; Laffin JJ
Cancer Genet; 2013; 206(9-10):317-26. PubMed ID: 24269304
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
