323 related articles for article (PubMed ID: 17478934)
1. [Identification of the origin of marker chromosome by comparative genomic hybridization].
Zhou L; Wu LQ; Liang DS; Pan Q; Long ZG; Dai HP; Li J; Cai F; Xia K; Xia JH
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2007 Apr; 32(2):264-7. PubMed ID: 17478934
[TBL] [Abstract][Full Text] [Related]
2. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
Zunino A; Viaggi S; Ottaggio L; Fronza G; Schenone A; Roncella S; Abbondandolo A
Haematologica; 2000 Mar; 85(3):250-5. PubMed ID: 10702812
[TBL] [Abstract][Full Text] [Related]
3. Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.
Ness GO; Lybaek H; Houge G
Am J Med Genet; 2002 Nov; 113(2):125-36. PubMed ID: 12407702
[TBL] [Abstract][Full Text] [Related]
4. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
[TBL] [Abstract][Full Text] [Related]
5. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
[TBL] [Abstract][Full Text] [Related]
6. Genomic alterations in lung adenocarcinomas detected by multicolor fluorescence in situ hybridization and comparative genomic hybridization.
Shen H; Zhu Y; Wu YJ; Qiu HR; Shu YQ
Cancer Genet Cytogenet; 2008 Mar; 181(2):100-7. PubMed ID: 18295661
[TBL] [Abstract][Full Text] [Related]
7. [Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization].
Liang Y; Luo XP
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):435-7. PubMed ID: 16086285
[TBL] [Abstract][Full Text] [Related]
8. Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.
Vermeesch JR; Melotte C; Froyen G; Van Vooren S; Dutta B; Maas N; Vermeulen S; Menten B; Speleman F; De Moor B; Van Hummelen P; Marynen P; Fryns JP; Devriendt K
J Histochem Cytochem; 2005 Mar; 53(3):413-22. PubMed ID: 15750031
[TBL] [Abstract][Full Text] [Related]
9. [Multicolor fluorescence in situ hybridization (mFISH].
Michalová K; Zemanová Z; Brezinová J
Cas Lek Cesk; 2001 Mar; 140(4):99-103. PubMed ID: 11284431
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [The application and significance in prenatal diagnosis using G-banding, fluorescence in situ hybridization and comparative genomic hybridization].
Zhang WS; Chen QN; Wu XH; Liang QH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):156-60. PubMed ID: 19350506
[TBL] [Abstract][Full Text] [Related]
12. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
13. Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2.
Schoumans J; Johansson B; Corcoran M; Kuchinskaya E; Golovleva I; Grandér D; Forestier E; Staaf J; Borg A; Gustafsson B; Blennow E; Nordgren A
Br J Haematol; 2006 Nov; 135(4):492-9. PubMed ID: 16999846
[TBL] [Abstract][Full Text] [Related]
14. [Identification and characterization of marker chromosome in Turner syndrome].
Tan YQ; Cheng DH; DI YF; Li LY; Lu GX
Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543
[TBL] [Abstract][Full Text] [Related]
15. Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.
Li S; Malafiej P; Levy B; Mahmood R; Field M; Hughes T; Lockhart LH; Wu Z; Huang M; Hirschhorn K; Velagaleti GV; Daniel A; Warburton PE
Am J Med Genet; 2002 Jul; 110(3):258-67. PubMed ID: 12116235
[TBL] [Abstract][Full Text] [Related]
16. Comparative genomic hybridization (CGH) and fluorescence in situ hybridization (FISH) in the diagnosis of hepatocellular carcinoma.
Wilkens L; Bredt M; Flemming P; Mengel M; Becker T; Klempnauer J; Kreipe H
J Hepatobiliary Pancreat Surg; 2002; 9(3):304-11. PubMed ID: 12353141
[TBL] [Abstract][Full Text] [Related]
17. The cytogenetic view of standard comparative genomic hybridization (CGH): deletions of 20q in human leukemia as a measure of the sensitivity of the technique.
Brecevic L; Verdorfer I; Saul W; Trautmann U; Gebhart E
Anticancer Res; 2001; 21(1A):89-92. PubMed ID: 11299794
[TBL] [Abstract][Full Text] [Related]
18. CGH and direct diagnosis of mosaic structural chromosomal abnormalities: description of a mosaic ring chromosome 17 and review of the literature.
Dupont C; Pipiras E; Chantot-Bastaraud S; Verloes A; Baumann C; Wolf JP; Benzacken B
Eur J Hum Genet; 2003 Jun; 11(6):452-6. PubMed ID: 12774038
[TBL] [Abstract][Full Text] [Related]
19. Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses.
Mairal A; Pinglier E; Gilbert E; Peter M; Validire P; Desjardins L; Doz F; Aurias A; Couturier J
Genes Chromosomes Cancer; 2000 Aug; 28(4):370-9. PubMed ID: 10862045
[TBL] [Abstract][Full Text] [Related]
20. [Fluorescence in situ hybridization identifies complex chromosomal aberrations in multiple myeloma].
Liu SY; Huang JW; Zhang J; Du HP; Jiang H; Li JY; Xue YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):685-8. PubMed ID: 18067084
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
