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Journal Abstract Search

102 related items for PubMed ID: 11568928

  • 1.
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  • 2. Interstitial deletion of the long arm of chromosome 4 [del(4)(q21.22q23)] and a liver tumor.
    Suwa K, Momoi MY, Yamagata T, Mori Y.
    Am J Med Genet; 1998 Jul 07; 78(3):291-3. PubMed ID: 9677069
    [Abstract] [Full Text] [Related]

  • 3. Comprehensive allelotyping of hepatoblastoma.
    Terada Y, Matsumoto S, Bando K, Tajiri T.
    Hepatogastroenterology; 2009 Jul 07; 56(89):199-204. PubMed ID: 19453057
    [Abstract] [Full Text] [Related]

  • 4. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech.
    Bonnet C, Andrieux J, Béri-Dexheimer M, Leheup B, Boute O, Manouvrier S, Delobel B, Copin H, Receveur A, Mathieu M, Thiriez G, Le Caignec C, David A, de Blois MC, Malan V, Philippe A, Cormier-Daire V, Colleaux L, Flori E, Dollfus H, Pelletier V, Thauvin-Robinet C, Masurel-Paulet A, Faivre L, Tardieu M, Bahi-Buisson N, Callier P, Mugneret F, Edery P, Jonveaux P, Sanlaville D.
    J Med Genet; 2010 Jun 07; 47(6):377-84. PubMed ID: 20522426
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  • 5. 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 07; 34(9):864-71. PubMed ID: 14562281
    [Abstract] [Full Text] [Related]

  • 6. 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 07; 19(4):291-4. PubMed ID: 9258666
    [Abstract] [Full Text] [Related]

  • 7. Hepatic Malignancy in an Infant with Wolf-Hirschhorn Syndrome.
    Rutter S, Morotti RA, Peterec S, Gallagher PG.
    Fetal Pediatr Pathol; 2017 Jun 07; 36(3):256-262. PubMed ID: 28266898
    [Abstract] [Full Text] [Related]

  • 8. Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype.
    Velinov M, Kupferman J, Gu H, Macera MJ, Babu A, Jenkins EC, Kupchik G.
    Eur J Med Genet; 2005 Jun 07; 48(1):51-5. PubMed ID: 15953406
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  • 12. Comparative genomic hybridization reveals population-based genetic alterations in hepatoblastomas.
    Gray SG, Kytölä S, Matsunaga T, Larsson C, Ekström TJ.
    Br J Cancer; 2000 Oct 07; 83(8):1020-5. PubMed ID: 10993649
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  • 13. 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 07; 34(3):165-70. PubMed ID: 10696121
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  • 14. 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 07; 11(3):199-202. PubMed ID: 7530489
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  • 16. [2q21-qter trisomy in hepatoblastoma].
    Balogh E, Swanton S, Kiss C, Jakab Z, Secker-Walker LM, Oláh E.
    Orv Hetil; 1997 Dec 14; 138(50):3179-83. PubMed ID: 9446083
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  • 18. Amplification of 4q21-q22 and the MXR gene in independently derived mitoxantrone-resistant cell lines.
    Knutsen T, Rao VK, Ried T, Mickley L, Schneider E, Miyake K, Ghadimi BM, Padilla-Nash H, Pack S, Greenberger L, Cowan K, Dean M, Fojo T, Bates S.
    Genes Chromosomes Cancer; 2000 Jan 14; 27(1):110-6. PubMed ID: 10564593
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  • 20. Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly.
    Kulharya AS, Maberry M, Kukolich MK, Day DW, Schneider NR, Wilson GN, Tonk V.
    Am J Med Genet; 1995 Jan 16; 55(2):165-70. PubMed ID: 7717415
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