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Journal Abstract Search
242 related items for PubMed ID: 11295135
1. [Application of chromosome painting technique to analysis of structural aberration of human chromosomes]. Yang H, Song Y, Liu Q, Li Y, Fu S, Zhang G, Li P. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr; 18(2):135-8. PubMed ID: 11295135 [Abstract] [Full Text] [Related]
2. [Application of chromosome painting to analysis of structural aberration in five cases]. Su G, Qiao H, Shi Z, Su R, Zeng X, Zhao F, Yang H, Huang S. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Aug; 15(4):202-5. PubMed ID: 9691125 [Abstract] [Full Text] [Related]
3. [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 [Abstract] [Full Text] [Related]
4. [Study of a familial insertional translocation involving chromosomes 1 and 7 by using fluorescence in situ hybridization]. Tan Y, Li X, Li L, Lu G. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun; 18(3):183-6. PubMed ID: 11402445 [Abstract] [Full Text] [Related]
5. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization]. Huang Y, Sun X, Li Q. Zhonghua Yi Xue Za Zhi; 1999 Feb; 79(2):106-8. PubMed ID: 11601014 [Abstract] [Full Text] [Related]
6. Accurate detection of true incomplete exchanges in human lymphocytes exposed to neutron radiation using chromosome painting in combination with a telomeric PNA probe. Fomina J, Darroudi F, Natarajan AT. Int J Radiat Biol; 2001 Dec; 77(12):1175-83. PubMed ID: 11747542 [Abstract] [Full Text] [Related]
7. 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 [Abstract] [Full Text] [Related]
8. A new chromosome banding technique, spectral color banding (SCAN), for full characterization of chromosomal abnormalities. Kakazu N, Bar-Am I, Hada S, Ago H, Abe T. Genes Chromosomes Cancer; 2003 Aug; 37(4):412-6. PubMed ID: 12800153 [Abstract] [Full Text] [Related]
9. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH. Schoch C, Haferlach T, Bursch S, Gerstner D, Schnittger S, Dugas M, Kern W, Löffler H, Hiddemann W. Genes Chromosomes Cancer; 2002 Sep; 35(1):20-9. PubMed ID: 12203786 [Abstract] [Full Text] [Related]
10. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia. Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S. Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352 [Abstract] [Full Text] [Related]
11. [Analysis of a case of balanced chromosome translocation and phenotypic abnormality by fluorescence in situ hybridization]. Zhu G, Bartsch O, Wan M, Gillessen-Kaesbach G, Passarge E. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr; 18(2):96-9. PubMed ID: 11295125 [Abstract] [Full Text] [Related]
12. Fluorescene in situ hybridization establishes homology between human and silvered leaf monkey chromosomes, reveals reciprocal translocations between chromosomes homologous to human Y/5, 1/9, and 6/16, and delineates an X1X2Y1Y2/X1X1X2X2 sex-chromosome system. Bigoni F, Koehler U, Stanyon R, Ishida T, Wienberg J. Am J Phys Anthropol; 1997 Mar; 102(3):315-27. PubMed ID: 9098501 [Abstract] [Full Text] [Related]
13. Chromosomal cryptic insertion of the terminal region and its formative mechanism determined by fluorescence in situ hybridization. Tan Y, Lu G. Chin Med J (Engl); 2002 Jul; 115(7):1039-42. PubMed ID: 12150739 [Abstract] [Full Text] [Related]
15. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies. Frenny VJ, Antonella Z, Luisa A, Shah AD, Sheth JJ, Rocchi M. Indian J Cancer; 2003 Jul; 40(4):135-9. PubMed ID: 14716109 [Abstract] [Full Text] [Related]
16. [A study on complicated chromosome translocation by fluorescence in situ hybridization (FISH) of G-banded chromosomes]. Huang H, Zhang X, Chen Y, Cui Y. Yi Chuan Xue Bao; 1996 Jul; 23(5):338-42. PubMed ID: 9041776 [Abstract] [Full Text] [Related]
17. [Selective chromosome painting using in situ hybridization]. Pérez Losada A, Woessner S, Solé F, Caballín MR, Florensa L. Sangre (Barc); 1993 Apr; 38(2):151-4. PubMed ID: 8516730 [Abstract] [Full Text] [Related]
18. 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 [Abstract] [Full Text] [Related]
19. [Application of fluorescence insitu hybridization technique for prenatal diagnosis of chromosome abnormality in amniotic cells]. Huang Y, Sun X, Li Q. Zhonghua Fu Chan Ke Za Zhi; 1999 Mar; 34(3):153-5. PubMed ID: 11263185 [Abstract] [Full Text] [Related]