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Journal Abstract Search

185 related items for PubMed ID: 10696121

  • 41. Translocations between the long arms of chromosomes 1 and 5 in hematologic malignancies are strongly associated with neoplasms of the myeloid lineages.
    Johansson B, Brøndum-Nielsen K, Billström R, Schiødt I, Mitelman F.
    Cancer Genet Cytogenet; 1997 Dec; 99(2):97-101. PubMed ID: 9398862
    [Abstract] [Full Text] [Related]

  • 42. Comparative genomic hybridization analysis of hepatoblastoma reveals high frequency of X-chromosome gains and similarities between epithelial and stromal components.
    Terracciano LM, Bernasconi B, Ruck P, Stallmach T, Briner J, Sauter G, Moch H, Vecchione R, Pollice L, Pettinato G, Gürtl B, Ratschek M, De Krijger R, Tornillo L, Bruder E.
    Hum Pathol; 2003 Sep; 34(9):864-71. PubMed ID: 14562281
    [Abstract] [Full Text] [Related]

  • 43. Gain of chromosome arm 1q in patients in relapse and progression of multiple myeloma.
    Balcárková J, Urbánková H, Scudla V, Holzerová M, Bacovský J, Indrák K, Jarosová M.
    Cancer Genet Cytogenet; 2009 Jul 15; 192(2):68-72. PubMed ID: 19596256
    [Abstract] [Full Text] [Related]

  • 44. Chromosomal aberrations during progression of chronic myeloid leukemia identified by cytogenetic and molecular cytogenetic tools: implication of 1q12-21.
    Su XY, Wong N, Cao Q, Yu LZ, Niu C, Wickham N, Johnson PJ, Chen Z, Chen SJ.
    Cancer Genet Cytogenet; 1999 Jan 01; 108(1):6-12. PubMed ID: 9973917
    [Abstract] [Full Text] [Related]

  • 45. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
    Lestou VS, Ludkovski O, Connors JM, Gascoyne RD, Lam WL, Horsman DE.
    Genes Chromosomes Cancer; 2003 Apr 01; 36(4):375-81. PubMed ID: 12619161
    [Abstract] [Full Text] [Related]

  • 46. 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]

  • 47. Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent-1 segregants.
    Kozma C, Slavotinek AM, Meck JM.
    Am J Med Genet A; 2004 Jan 15; 124A(2):118-28. PubMed ID: 14699608
    [Abstract] [Full Text] [Related]

  • 48. 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 15; 111(9):1545-50. PubMed ID: 11568603
    [Abstract] [Full Text] [Related]

  • 49. Rearrangement of chromosome 1 is a frequent finding in endometrial carcinoma. An in situ hybridization study in nine endometrial carcinomas.
    Ketter R, von Ballestrem CL, Lampel S, Seitz G, Zang KD, Romanakis K, Wullich B.
    Cancer Genet Cytogenet; 1995 Jun 15; 81(2):109-14. PubMed ID: 7621405
    [Abstract] [Full Text] [Related]

  • 50. Fetal-type hepatoblastoma and del(3)(q11.2q13.2).
    Sandoval C, Piper J, Mowery-Rushton PA, Jayabose S.
    Cancer Genet Cytogenet; 2002 Apr 15; 134(2):162-4. PubMed ID: 12034532
    [Abstract] [Full Text] [Related]

  • 51. Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.
    Xu W, Li JY, Liu Q, Zhu Y, Pan JL, Qiu HR, Xue YQ.
    Int J Lab Hematol; 2010 Feb 15; 32(1 Pt 1):e86-95. PubMed ID: 20089000
    [Abstract] [Full Text] [Related]

  • 52. 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 15; 21(11):1381-6. PubMed ID: 9351578
    [Abstract] [Full Text] [Related]

  • 53. 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 15; 85(3):250-5. PubMed ID: 10702812
    [Abstract] [Full Text] [Related]

  • 54. Characterization of genomic alterations in hepatoblastomas. A role for gains on chromosomes 8q and 20 as predictors of poor outcome.
    Weber RG, Pietsch T, von Schweinitz D, Lichter P.
    Am J Pathol; 2000 Aug 15; 157(2):571-8. PubMed ID: 10934159
    [Abstract] [Full Text] [Related]

  • 55.
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  • 56. Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.
    Röthlisberger B, Kotzot D, Brecevic L, Koehler M, Balmer D, Binkert F, Schinzel A.
    Eur J Hum Genet; 1999 Dec 15; 7(8):873-83. PubMed ID: 10602362
    [Abstract] [Full Text] [Related]

  • 57. [Terminal 1q deletion by translocation t(1;20)pat, confirmed by in situ hybridization].
    López-Ginés C, Gil-Benso R, Gregori-Romero MA, Paredes-Cencillo C, Castelló-Pomares M, Llombart-Bosch A.
    An Esp Pediatr; 1998 Mar 15; 48(3):309-11. PubMed ID: 9608096
    [No Abstract] [Full Text] [Related]

  • 58. Molecular cytogenetic analysis of 1;17 translocations in neuroblastoma.
    Van Roy N, Cheng NC, Laureys G, Opdenakker G, Versteeg R, Speleman F.
    Eur J Cancer; 1995 Mar 15; 31A(4):530-5. PubMed ID: 7576960
    [Abstract] [Full Text] [Related]

  • 59. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.
    Sifakis S, Eleftheriades M, Kappou D, Murru R, Konstantinidou A, Orru S, Ziegler M, Liehr T, Manolakos E, Papoulidis I.
    Birth Defects Res A Clin Mol Teratol; 2014 Apr 15; 100(4):284-93. PubMed ID: 24677675
    [Abstract] [Full Text] [Related]

  • 60. Detailed analysis of 26 cases of 1q partial duplication/triplication syndrome.
    Watanabe S, Shimizu K, Ohashi H, Kosaki R, Okamoto N, Shimojima K, Yamamoto T, Chinen Y, Mizuno S, Dowa Y, Shiomi N, Toda Y, Tashiro K, Shichijo K, Minatozaki K, Aso S, Minagawa K, Hiraki Y, Shimokawa O, Matsumoto T, Fukuda M, Moriuchi H, Yoshiura K, Kondoh T.
    Am J Med Genet A; 2016 Apr 15; 170A(4):908-17. PubMed ID: 26782913
    [Abstract] [Full Text] [Related]

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