184 related articles for article (PubMed ID: 10705876)
1. Fluorescence in situ hybridization: molecular probes for diagnosis of pediatric neoplastic diseases.
Raimondi SC
Cancer Invest; 2000; 18(2):135-47. PubMed ID: 10705876
[TBL] [Abstract][Full Text] [Related]
2. Detection of chromosomal abnormalities using fluorescence in situ hybridization (FISH).
Jobanputra V; Kriplani A; Choudhry VP; Kucheria K
Natl Med J India; 1998; 11(6):259-63. PubMed ID: 10083791
[TBL] [Abstract][Full Text] [Related]
3. Fluorescence in situ hybridization: uses and limitations.
Gozzetti A; Le Beau MM
Semin Hematol; 2000 Oct; 37(4):320-33. PubMed ID: 11071355
[TBL] [Abstract][Full Text] [Related]
4. Applications of Fluorescence In Situ Hybridization Technology in Malignancies.
Tansatit M
Methods Mol Biol; 2017; 1541():75-90. PubMed ID: 27910016
[TBL] [Abstract][Full Text] [Related]
5. Molecular cytogenetic applications in analysis of the cancer genome.
Rao PH; Nandula SV; Murty VV
Methods Mol Biol; 2007; 383():165-85. PubMed ID: 18217685
[TBL] [Abstract][Full Text] [Related]
6. [Contribution of molecular cytogenetics in the diagnosis of chromosomal abnormalities].
Bouayed Abdelmoula N
Ann Biol Clin (Paris); 2004; 62(6):629-37. PubMed ID: 15563421
[TBL] [Abstract][Full Text] [Related]
7. Cytogenetics and cancer.
Patel AS; Hawkins AL; Griffin CA
Curr Opin Oncol; 2000 Jan; 12(1):62-7. PubMed ID: 10687731
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Advanced molecular and cytogenetic technologies in birth defect diagnosis and prevention.
Li MM
Beijing Da Xue Xue Bao Yi Xue Ban; 2005 Feb; 37(1):14-9. PubMed ID: 15719034
[TBL] [Abstract][Full Text] [Related]
10. Fluorescent in situ hybridization as an adjunct to conventional cytogenetics.
Mark HF
Ann Clin Lab Sci; 1994; 24(2):153-63. PubMed ID: 8203823
[TBL] [Abstract][Full Text] [Related]
11. Effectiveness of prenatal chromosomal analysis using multicolor fluorescent in situ hybridisation.
Thilaganathan B; Sairam S; Ballard T; Peterson C; Meredith R
BJOG; 2000 Feb; 107(2):262-6. PubMed ID: 10688511
[TBL] [Abstract][Full Text] [Related]
12. Molecular cytogenetics: an indispensable tool for cancer diagnosis.
Wan TS; Ma ES
Chang Gung Med J; 2012; 35(2):96-110. PubMed ID: 22537925
[TBL] [Abstract][Full Text] [Related]
13. Utility of multicolor fluorescent in situ hybridization in clinical cytogenetics.
Jalal SM; Law ME
Genet Med; 1999; 1(5):181-6. PubMed ID: 11256670
[TBL] [Abstract][Full Text] [Related]
14. [Current methods of molecular cytogenetics in pre- and postnatal diagnosis of chromosome aberrations].
Vorsanova SG; Iurov IuB; Solov'ev IV; Demidova IA; Sharonin VO; Male R; Zhiollant M; Beresheva AK; Kolotiĭ AD; Kravets VS; Ruazes Zh
Klin Lab Diagn; 2000 Aug; (8):36-9. PubMed ID: 11031431
[TBL] [Abstract][Full Text] [Related]
15. [Impact of tumorcytogenetics in tumor diagnostics].
Wenzel F; Röthlisberger B
Ther Umsch; 2008 Sep; 65(9):473-80. PubMed ID: 18791960
[TBL] [Abstract][Full Text] [Related]
16. [Molecular cytogenetic techniques and their application in clinical diagnosis].
Nowakowska B; Bocian E
Med Wieku Rozwoj; 2004; 8(1):7-24. PubMed ID: 15557693
[TBL] [Abstract][Full Text] [Related]
17. Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease.
Stumm M; Tönnies H; Wieacker PF
Eur J Pediatr; 1999 Jul; 158(7):531-6. PubMed ID: 10412808
[TBL] [Abstract][Full Text] [Related]
18. [Genes and chromosomes: imaging in genetics].
Jonveaux P
Rev Prat; 1997 Jan; 47(2):140-5. PubMed ID: 9157511
[TBL] [Abstract][Full Text] [Related]
19. Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridization.
Gribble SM; Roberts I; Grace C; Andrews KM; Green AR; Nacheva EP
Cancer Genet Cytogenet; 2000 Apr; 118(1):1-8. PubMed ID: 10731582
[TBL] [Abstract][Full Text] [Related]
20. Detection of chromosomal abnormalities in uterine leiomyoma using conventional cytogenetic method and interphase fluorescence in situ hybridization.
Hayashi S; Miharu N; Okamoto E; Samura O; Hara T; Ohama K
Cancer Genet Cytogenet; 1996 Jul; 89(2):98-104. PubMed ID: 8697434
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
