BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 2095703)

  • 1. Reassessment of two apparent deletions of chromosome 16p to an ins(11;16) and a t(1;16) by chromosome painting.
    Callen DF; Baker E; Eyre HJ; Chernos JE; Bell JA; Sutherland GR
    Ann Genet; 1990; 33(4):219-21. PubMed ID: 2095703
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comparative genomic hybridization study of primary neuroblastoma tumors. United Kingdom Children's Cancer Study Group.
    Lastowska M; Nacheva E; McGuckin A; Curtis A; Grace C; Pearson A; Bown N
    Genes Chromosomes Cancer; 1997 Mar; 18(3):162-9. PubMed ID: 9071568
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL.
    Brown J; Horsley SW; Jung C; Saracoglu K; Janssen B; Brough M; Daschner M; Beedgen B; Kerkhoffs G; Eils R; Harris PC; Jauch A; Kearney L
    Eur J Hum Genet; 2000 Dec; 8(12):903-10. PubMed ID: 11175277
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interstitial deletion of bands 11q21-->22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes.
    Horelli-Kuitunen N; Gahmberg N; Eeva M; Palotie A; Järvelä I
    Am J Med Genet; 1999 Oct; 86(5):416-9. PubMed ID: 10508981
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Use of fluorescence in situ hybridization to clarify a complex chromosomal rearrangement in a child with multiple congenital anomalies.
    Spikes AS; Hegmann K; Smith JL; Shaffer LG
    Am J Med Genet; 1995 May; 57(1):31-4. PubMed ID: 7645595
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Reciprocal translocation t(1;15)(p36.2;p11.2): confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p).
    Barbi G; Kennerknecht I; Klett C
    Am J Med Genet; 1992 Jul; 43(4):722-5. PubMed ID: 1621764
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Applications of comparative genomic hybridisation in constitutional chromosome studies.
    Breen CJ; Barton L; Carey A; Dunlop A; Glancy M; Hall K; Hegarty AM; Khokhar MT; Power M; Ryan K; Green AJ; Stallings RL
    J Med Genet; 1999 Jul; 36(7):511-7. PubMed ID: 10424810
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21.
    McGinniss MJ; Rosenberg C; Stetten G; Schinzel AA; Binkert F; Petersen MB; Kearns WG; Kazazian HH; Pearson PL; Antonarakis SE
    Am J Med Genet; 1993 Jul; 46(6):647-51. PubMed ID: 8362906
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytogenetic study of a patient with infant acute lymphoblastic leukemia using GTG-banding and chromosome painting.
    Alter D; Mark HF
    Exp Mol Pathol; 2000 Oct; 69(2):152-8. PubMed ID: 11001863
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers.
    Filippova GN; Lindblom A; Meincke LJ; Klenova EM; Neiman PE; Collins SJ; Doggett NA; Lobanenkov VV
    Genes Chromosomes Cancer; 1998 May; 22(1):26-36. PubMed ID: 9591631
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization.
    Engelen JJ; Loots WJ; Albrechts JC; Plomp AS; van der Meer SB; Vles JS; Hamers GJ; Geraedts JP
    Am J Med Genet; 1998 Feb; 75(4):409-13. PubMed ID: 9482648
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosome 12 breakpoints are cytogenetically different in benign and malignant lipogenic tumors: localization of breakpoints in lipoma to 12q15 and in myxoid liposarcoma to 12q13.3.
    Mrózek K; Karakousis CP; Bloomfield CD
    Cancer Res; 1993 Apr; 53(7):1670-5. PubMed ID: 8453640
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
    Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16p13.3 by a de novo reciprocal translocation, t(7;16)(q34;p13.3).
    Tommerup N; van der Hagen CB; Heiberg A
    Am J Med Genet; 1992 Sep; 44(2):237-41. PubMed ID: 1456298
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cytogenetic findings in a breast stromal sarcoma. Application of fluorescence in situ hybridization to characterize the breakpoint regions in an 11;19 translocation.
    Garcia-Palazzo IE; Palazzo JP; Liu ZM; Taguchi T; Testa JR
    Cancer Genet Cytogenet; 1992 Oct; 63(1):47-51. PubMed ID: 1423226
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Instability of chromosomes 1, 3, 16, and 17 in primary breast carcinomas inferred by fluorescence in situ hybridization.
    Anamthawat-Jónsson K; Eyfjörd JE; Ogmundsdóttir HM; Pétursdóttir I; Steinarsdóttir M
    Cancer Genet Cytogenet; 1996 May; 88(1):1-7. PubMed ID: 8630972
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosome 1q terminal deletion resulting from de novo translocation with an acrocentric chromosome.
    Arai E; Nishimura S; Tamura K; Kida M; Ikeuchi T
    Jpn J Hum Genet; 1994 Dec; 39(4):433-7. PubMed ID: 7873756
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Application of micro-FISH to delineate deletions.
    Engelen JJ; Albrechts JC; Loots WJ; Hollanders-Crombach BH; Hamers AJ; Geraedts JP
    Cytogenet Cell Genet; 1996; 75(2-3):167-71. PubMed ID: 9040786
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.