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Journal Abstract Search

138 related items for PubMed ID: 9258666

  • 1. The first recurring chromosome translocation in hepatoblastoma: der(4)t(1;4)(q12;q34).
    Schneider NR, Cooley LD, Finegold MJ, Douglass EC, Tomlinson GE.
    Genes Chromosomes Cancer; 1997 Aug; 19(4):291-4. PubMed ID: 9258666
    [Abstract] [Full Text] [Related]

  • 2. Cytogenetic characterization of childhood hepatoblastoma.
    Ma SK, Cheung AN, Choy C, Chan GC, Ha SY, Ching LM, Wan TS, Chan LC.
    Cancer Genet Cytogenet; 2000 May; 119(1):32-6. PubMed ID: 10812168
    [Abstract] [Full Text] [Related]

  • 3. Trisomy 1q, 2, and 20 in a case of hepatoblastoma: possible significance of 2q35-q37 and 1q12-q21 rearrangements.
    Yeh YA, Rao PH, Cigna CT, Middlesworth W, Lefkowitch JH, Murty VV.
    Cancer Genet Cytogenet; 2000 Dec; 123(2):140-3. PubMed ID: 11150606
    [Abstract] [Full Text] [Related]

  • 4. Cytogenetic evaluation of a large series of hepatoblastomas: numerical abnormalities with recurring aberrations involving 1q12-q21.
    Tomlinson GE, Douglass EC, Pollock BH, Finegold MJ, Schneider NR.
    Genes Chromosomes Cancer; 2005 Oct; 44(2):177-84. PubMed ID: 15981236
    [Abstract] [Full Text] [Related]

  • 5. Cytogenetic findings in two new cases of hepatoblastoma.
    Ali W, Savasan S, Rabah R, Mohamed AN.
    Cancer Genet Cytogenet; 2002 Mar; 133(2):179-82. PubMed ID: 11943350
    [Abstract] [Full Text] [Related]

  • 6. Cytogenetic abnormalities and clonal evolution in an adult hepatoblastoma.
    Parada LA, Bardi G, Hallén M, Hägerstrand I, Tranberg KG, Mitelman F, Johansson B.
    Am J Surg Pathol; 1997 Nov; 21(11):1381-6. PubMed ID: 9351578
    [Abstract] [Full Text] [Related]

  • 7. Cytogenetic and array comparative genomic hybridization analysis of a series of hepatoblastomas.
    Stejskalová E, Malis J, Snajdauf J, Pýcha K, Urbánková H, Bajciová V, Starý J, Kodet R, Jarosová M.
    Cancer Genet Cytogenet; 2009 Oct 15; 194(2):82-7. PubMed ID: 19781440
    [Abstract] [Full Text] [Related]

  • 8. Cytogenetic abnormalities in hepatoblastoma: report of two new cases and review of the literature suggesting imbalance of chromosomal regions on chromosomes 1, 4, and 12.
    Nagata T, Nakamura M, Shichino H, Chin M, Sugito K, Ikeda T, Koshinaga T, Fukuzawa M, Inoue M, Mugishima H.
    Cancer Genet Cytogenet; 2005 Jan 01; 156(1):8-13. PubMed ID: 15588850
    [Abstract] [Full Text] [Related]

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  • 10. Significance of extra copies of chromosome 20 and the long arm of chromosome 2 in hepatoblastoma.
    Swarts S, Wisecarver J, Bridge JA.
    Cancer Genet Cytogenet; 1996 Oct 01; 91(1):65-7. PubMed ID: 8908169
    [Abstract] [Full Text] [Related]

  • 11. Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study.
    Parada LA, Limon J, Iliszko M, Czauderna P, Gisselsson D, Höglund M, Kullendorff CM, Wiebe T, Mertens F, Johansson B.
    Med Pediatr Oncol; 2000 Mar 01; 34(3):165-70. PubMed ID: 10696121
    [Abstract] [Full Text] [Related]

  • 12. Karyotypic analyses of hepatoblastoma. Report of two cases and review of the literature suggesting chromosomal loci responsible for the pathogenesis of this disease.
    Nagata T, Mugishima H, Shichino H, Suzuki T, Chin M, Koshinaga S, Inoue M, Harada K.
    Cancer Genet Cytogenet; 1999 Oct 01; 114(1):42-50. PubMed ID: 10526534
    [Abstract] [Full Text] [Related]

  • 13. Trisomy 2, trisomy 20, and del(17p) as sole chromosomal abnormalities in three cases of hepatoblastoma.
    Tonk VS, Wilson KS, Timmons CF, Schneider NR.
    Genes Chromosomes Cancer; 1994 Nov 01; 11(3):199-202. PubMed ID: 7530489
    [Abstract] [Full Text] [Related]

  • 14. Trisomy 2 and 19, and tetrasomy 1q and 14 in hepatoblastoma.
    Park JP, Ornvold KT, Brown AM, Mohandas TK.
    Cancer Genet Cytogenet; 1999 Nov 01; 115(1):86-7. PubMed ID: 10565309
    [No Abstract] [Full Text] [Related]

  • 15. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
    Chen Z, Grebe TA, Guan XY, Notohamiprodjo M, Nutting PJ, Stone JF, Trent JM, Sandberg AA.
    Am J Med Genet; 1997 Aug 08; 71(2):160-6. PubMed ID: 9217215
    [Abstract] [Full Text] [Related]

  • 16. Cytogenetic analysis of hepatoblastoma: hypothesis of cytogenetic evolution in such tumors and results of a multicentric study.
    Sainati L, Leszl A, Stella M, Montaldi A, Perilongo G, Rugge M, Bolcato S, Iolascon A, Basso G.
    Cancer Genet Cytogenet; 1998 Jul 01; 104(1):39-44. PubMed ID: 9648556
    [Abstract] [Full Text] [Related]

  • 17. Acute megakaryoblastic leukemia with t(1;22)(p13.3;q13.1); RBM15-MKL1 mimicking hepatoblastoma in an infant: The role of karyotype in differential diagnosis.
    Marques-Piubelli ML, Cordeiro MG, Cristofani L, Barroso RS, Paes VR, Castelli JB, Rodrigues Pereira Velloso ED.
    Pediatr Blood Cancer; 2020 Mar 01; 67(3):e28111. PubMed ID: 31802626
    [No Abstract] [Full Text] [Related]

  • 18. Undifferentiated small cell hepatoblastoma with a chromosomal translocation t(22;22)(q11;q13).
    Gunawan B, Schäfer KL, Sattler B, Lorf T, Dockhorn-Dworniczak B, Ringe B, Füzesi L.
    Histopathology; 2002 May 01; 40(5):485-7. PubMed ID: 12010372
    [No Abstract] [Full Text] [Related]

  • 19. Fluorescent in situ hybridization (FISH) reveals frequent and recurrent numerical and structural abnormalities in hepatoblastoma with no informative karyotype.
    Surace C, Leszl A, Perilongo G, Rocchi M, Basso G, Sainati L.
    Med Pediatr Oncol; 2002 Nov 01; 39(5):536-9. PubMed ID: 12228913
    [Abstract] [Full Text] [Related]

  • 20. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature.
    Wang CB, Lin SP, Chen CP, Chen YJ, Lee CC.
    Genet Couns; 2006 Nov 01; 17(4):435-40. PubMed ID: 17375530
    [Abstract] [Full Text] [Related]

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