BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 2821320)

  • 1. [Wiedemann-Beckwith syndrome: clinical characteristics, constitutional chromosome abnormalities and tumor incidence].
    Haas OA; Zoubek A; Grümayer ER; Ferstl G; Gadner H
    Klin Padiatr; 1987; 199(4):283-91. PubMed ID: 2821320
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma.
    Haas OA; Zoubek A; Grümayer ER; Gadner H
    Cancer Genet Cytogenet; 1986 Oct; 23(2):95-104. PubMed ID: 3019515
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
    Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
    Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors.
    Kaneko Y; Homma C; Maseki N; Sakurai M; Hata J
    Cancer Res; 1991 Nov; 51(21):5937-42. PubMed ID: 1657374
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5).
    Norman AM; Read AP; Clayton-Smith J; Andrews T; Donnai D
    Am J Med Genet; 1992 Feb; 42(4):638-41. PubMed ID: 1609847
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24).
    Gadzicki D; Baumer A; Wey E; Happel CM; Rudolph C; Tönnies H; Neitzel H; Steinemann D; Welte K; Klein C; Schlegelberger B
    Ann Hum Genet; 2006 Nov; 70(Pt 6):958-64. PubMed ID: 17044870
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
    Fryns JP; Kleczkowska A; Devriendt K; Devliegher H; Van den Berghe H
    Genet Couns; 1993; 4(1):37-41. PubMed ID: 8471219
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosome abnormalities in tumor cells from patients with sporadic Wilms' tumor.
    Kondo K; Chilcote RR; Maurer HS; Rowley JD
    Cancer Res; 1984 Nov; 44(11):5376-81. PubMed ID: 6091875
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Cytogenetic aspects of pediatric germ cell tumors].
    Stock C; Ambros IM; Strehl S; Zoubek A; Fink FM; Gadner H; Ambros PF
    Klin Padiatr; 1995; 207(4):235-41. PubMed ID: 7564160
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Constitutional chromosome anomalies in patients with cerebral gigantism (Sotos syndrome).
    Haeusler G; Guchev Z; Köhler I; Schober E; Haas O; Frisch H
    Klin Padiatr; 1993; 205(5):351-3. PubMed ID: 8411901
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
    Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Abnormalities of chromosome 1 and loss of heterozygosity on 1p in primary hepatomas.
    Simon D; Knowles BB; Weith A
    Oncogene; 1991 May; 6(5):765-70. PubMed ID: 1646986
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Frequent multiplication of the long arm of chromosome 8 in hepatocellular carcinoma.
    Fujiwara Y; Monden M; Mori T; Nakamura Y; Emi M
    Cancer Res; 1993 Feb; 53(4):857-60. PubMed ID: 8381331
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Nonrandom chromosomal changes in transitional cell carcinoma of the bladder.
    Gibas Z; Prout GR; Connolly JG; Pontes JE; Sandberg AA
    Cancer Res; 1984 Mar; 44(3):1257-64. PubMed ID: 6692407
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Cytogenetic studies in Wilm's tumor].
    Balogh E; Oláh E; Kovács I; Pásti G
    Orv Hetil; 1990 Dec; 131(52):2863-6. PubMed ID: 2177179
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new cases.
    Journel H; Lucas J; Allaire C; Le Mée F; Defawe G; Lecornu M; Jouan H; Roussey M; Le Marec B
    Ann Genet; 1985; 28(2):97-101. PubMed ID: 3876070
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.
    Kubota T; Saitoh S; Matsumoto T; Narahara K; Fukushima Y; Jinno Y; Niikawa N
    Am J Med Genet; 1994 Feb; 49(4):378-83. PubMed ID: 7909196
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Complex chromosome rearrangements and congenital anomalies.
    Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
    Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 156(1):8-13. PubMed ID: 15588850
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.