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    Results: 12

    1.

    Chromosome 3 status in uveal melanoma: a comparison of fluorescence in situ hybridization and single-nucleotide polymorphism array.

    Singh AD, Aronow ME, Sun Y, Bebek G, Saunthararajah Y, Schoenfield LR, Biscotti CV, Tubbs RR, Triozzi PL, Eng C.

    Invest Ophthalmol Vis Sci. 2012 Jun 5;53(7):3331-9. doi: 10.1167/iovs.11-9027.

    PMID:
    22511634
    [PubMed - indexed for MEDLINE]

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    2.

    Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up study.

    Thomas S, Pütter C, Weber S, Bornfeld N, Lohmann DR, Zeschnigk M.

    Br J Cancer. 2012 Mar 13;106(6):1171-6. doi: 10.1038/bjc.2012.54. Epub 2012 Feb 21.

    PMID:
    22353812
    [PubMed - indexed for MEDLINE]
    Free PMC Article

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    3.

    Chromosome 3 anomalies investigated by genome wide SNP analysis of benign, low malignant potential and low grade ovarian serous tumours.

    Birch AH, Arcand SL, Oros KK, Rahimi K, Watters AK, Provencher D, Greenwood CM, Mes-Masson AM, Tonin PN.

    PLoS One. 2011;6(12):e28250. doi: 10.1371/journal.pone.0028250. Epub 2011 Dec 6.

    PMID:
    22163003
    [PubMed - indexed for MEDLINE]
    Free PMC Article

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    4.

    Paternal isodisomy of chromosome 3 unmasked by autosomal recessive microcoria-congenital nephrosis syndrome (Pierson syndrome) in a child with no other phenotypic abnormalities.

    Matejas V, Muscheites J, Wigger M, Kreutzer HJ, Nizze H, Zenker M.

    Am J Med Genet A. 2011 Oct;155A(10):2601-4. doi: 10.1002/ajmg.a.34214. Epub 2011 Sep 9. No abstract available.

    PMID:
    21910237
    [PubMed - indexed for MEDLINE]

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    5.

    Homozygous microdeletion of the POU1F1, CHMP2B, and VGLL3 genes in chromosome 3--a novel syndrome.

    Gat-Yablonski G, Frumkin-Ben David R, Bar M, Potievsky O, Phillip M, Lazar L.

    Am J Med Genet A. 2011 Sep;155A(9):2242-6. doi: 10.1002/ajmg.a.34136. Epub 2011 Aug 3.

    PMID:
    21815258
    [PubMed - indexed for MEDLINE]

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    6.

    A new lead from genetic studies in depressed siblings: assessing studies of chromosome 3.

    Hamilton SP.

    Am J Psychiatry. 2011 Aug;168(8):783-9. doi: 10.1176/appi.ajp.2011.11060835. Review.

    PMID:
    21813496
    [PubMed - indexed for MEDLINE]

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    7.

    A genome-wide significant linkage for severe depression on chromosome 3: the depression network study.

    Breen G, Webb BT, Butler AW, van den Oord EJ, Tozzi F, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen MJ, Cohen-Woods S, Perry J, Galwey NW, Upmanyu R, Craig I, Lewis CM, Ng M, Brewster S, Preisig M, Rietschel M, Jones L, Knight J, Rice J, Muglia P, Farmer AE, McGuffin P.

    Am J Psychiatry. 2011 Aug;168(8):840-7. doi: 10.1176/appi.ajp.2011.10091342. Epub 2011 May 15.

    PMID:
    21572164
    [PubMed - indexed for MEDLINE]

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    8.

    Frequency, molecular pathology and potential clinical significance of partial chromosome 3 aberrations in uveal melanoma.

    Abdel-Rahman MH, Christopher BN, Faramawi MF, Said-Ahmed K, Cole C, McFaddin A, Ray-Chaudhury A, Heerema N, Davidorf FH.

    Mod Pathol. 2011 Jul;24(7):954-62. doi: 10.1038/modpathol.2011.51. Epub 2011 Apr 15.

    PMID:
    21499235
    [PubMed - indexed for MEDLINE]
    Free Article

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    9.

    Mapping of genetic deletions on chromosome 3 in colorectal cancer: loss of 3p25-pter is associated with distant metastasis and poor survival.

    Tsai MH, Fang WH, Lin SH, Tzeng ST, Huang CS, Yen SJ, Chou SJ, Yang YC.

    Ann Surg Oncol. 2011 Sep;18(9):2662-70. doi: 10.1245/s10434-011-1603-9. Epub 2011 Feb 23.

    PMID:
    21347784
    [PubMed - indexed for MEDLINE]

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    10.

    5'-azacitidine in myelodysplastic syndromes with inversion of chromosome 3.

    Breccia M, Cannella L, Santopietro M, Loglisci G, Federico V, Salaroli A, Nanni M, Mancini M, Alimena G.

    Leukemia. 2011 Apr;25(4):736-7. doi: 10.1038/leu.2011.6. Epub 2011 Feb 4. No abstract available.

    PMID:
    21293489
    [PubMed - indexed for MEDLINE]

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    11.

    Whole-genome microarray detects deletions and loss of heterozygosity of chromosome 3 occurring exclusively in metastasizing uveal melanoma.

    Lake SL, Coupland SE, Taktak AF, Damato BE.

    Invest Ophthalmol Vis Sci. 2010 Oct;51(10):4884-91. doi: 10.1167/iovs.09-5083. Epub 2010 May 5.

    PMID:
    20445121
    [PubMed - indexed for MEDLINE]
    Free Article

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    12.

    Jumping translocation in acute monocytic leukemia (M5b) with alternative breakpoint sites in the long arm of donor chromosome 3.

    McGrattan P, Logan A, Humphreys M, Bowers M.

    Med Oncol. 2010 Sep;27(3):667-72. doi: 10.1007/s12032-009-9266-0. Epub 2009 Jul 22.

    PMID:
    19629764
    [PubMed - indexed for MEDLINE]

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