These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 3857964)

  • 1. Familial osteosarcoma associated with 13;14 chromosomal rearrangement.
    Gilman PA; Wang N; Fan SF; Reede J; Khan A; Leventhal BG
    Cancer Genet Cytogenet; 1985 Jun; 17(2):123-32. PubMed ID: 3857964
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas.
    Bayani J; Zielenska M; Pandita A; Al-Romaih K; Karaskova J; Harrison K; Bridge JA; Sorensen P; Thorner P; Squire JA
    Genes Chromosomes Cancer; 2003 Jan; 36(1):7-16. PubMed ID: 12461745
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.
    Yunis JJ; Ramsay NK
    J Pediatr; 1980 Jun; 96(6):1027-30. PubMed ID: 6246230
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic and spectral karyotype analyses of benign and malignant cartilage tumours.
    Sjögren H; Orndal C; Tingby O; Meis-Kindblom JM; Kindblom LG; Stenman G
    Int J Oncol; 2004 Jun; 24(6):1385-91. PubMed ID: 15138578
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lymphocyte chromosome survey in 80 patients with retinoblastoma.
    Mao WS; Lin XH; Ma QY; Chen YZ; Zeng LH; Dai ZY
    Yan Ke Xue Bao; 1989 Jun; 5(1-2):7-13. PubMed ID: 2485748
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosome analysis of nine osteosarcomas.
    Hoogerwerf WA; Hawkins AL; Perlman EJ; Griffin CA
    Genes Chromosomes Cancer; 1994 Feb; 9(2):88-92. PubMed ID: 7513549
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Solid tumors of children: chromosome abnormalities and the development of cancer.
    Gilbert F
    J Cell Physiol Suppl; 1984; 3():165-70. PubMed ID: 6086684
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytogenetic findings in 73 osteosarcoma specimens and a review of the literature.
    Bridge JA; Nelson M; McComb E; McGuire MH; Rosenthal H; Vergara G; Maale GE; Spanier S; Neff JR
    Cancer Genet Cytogenet; 1997 May; 95(1):74-87. PubMed ID: 9140456
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.
    Verma RS; Dosik H; Wexler IB
    J Genet Hum; 1977 Dec; 25(4):295-301. PubMed ID: 599332
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial pericentric inversion of chromosome 11 in a child with sporadic unilateral retinoblastoma.
    Ohnishi Y; Shigeto M; Ishibashi T; Hirata J
    Ophthalmic Paediatr Genet; 1990 Dec; 11(4):281-5. PubMed ID: 2096356
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cytogenetic aberrations in osteosarcomas. Nonrandom deletions, rings, and double-minute chromosomes.
    Fletcher JA; Gebhardt MC; Kozakewich HP
    Cancer Genet Cytogenet; 1994 Oct; 77(1):81-8. PubMed ID: 7923089
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cytogenetic findings in 19 malignant bone tumors.
    Ozisik YY; Meloni AM; Peier A; Altungoz O; Spanier SS; Zalupski MM; Leong SP; Sandberg AA
    Cancer; 1994 Oct; 74(8):2268-75. PubMed ID: 7922978
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cytogenetics of heritability in cancer.
    Evans HJ
    IARC Sci Publ; 1982; (39):35-56. PubMed ID: 6295935
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Monoallelic deletion of the p53 gene through chromosomal translocation in a small cell osteosarcoma.
    Nishio J; Gentry JD; Neff JR; Nelson M; Daniels W; Perry D; Gatalica Z; Bridge JA
    Virchows Arch; 2006 Jun; 448(6):852-6. PubMed ID: 16596382
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cytogenetic studies on fine-needle aspiration samples from osteosarcoma and Ewing's sarcoma.
    Akerman M; Dreinhöfer K; Rydholm A; Willén H; Mertens F; Mitelman F; Mandahl N
    Diagn Cytopathol; 1996 Jul; 15(1):17-22. PubMed ID: 8807247
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Combined spectral karyotyping, multicolor banding, and microarray comparative genomic hybridization analysis provides a detailed characterization of complex structural chromosomal rearrangements associated with gene amplification in the osteosarcoma cell line MG-63.
    Lim G; Karaskova J; Vukovic B; Bayani J; Beheshti B; Bernardini M; Squire JA; Zielenska M
    Cancer Genet Cytogenet; 2004 Sep; 153(2):158-64. PubMed ID: 15350306
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chromosomal abnormalities in human retinoblastoma. A review.
    Potluri VR; Helson L; Ellsworth RM; Reid T; Gilbert F
    Cancer; 1986 Aug; 58(3):663-71. PubMed ID: 3524791
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences.
    Trpchevska N; Dimova I; Arabadji T; Milachich T; Angelova S; Dimitrova M; Hristova-Savova M; Andreeva P; Timeva T; Shterev A
    J Assist Reprod Genet; 2017 May; 34(5):659-669. PubMed ID: 28236108
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes.
    Balaban G; Gilbert F; Nichols W; Meadows AT; Shields J
    Cancer Genet Cytogenet; 1982 Jul; 6(3):213-21. PubMed ID: 7116319
    [TBL] [Abstract][Full Text] [Related]  

  • 20. De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy.
    Fryns JP; Kleczkowska A; Kenis H
    Ann Genet; 1984; 27(1):62-4. PubMed ID: 6609678
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.