BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 15316976)

  • 1. Giant omphalocele and "prune belly" sequence as components of the Beckwith-Wiedemann syndrome.
    Sinico M; Touboul C; Haddad B; Encha-Razavi F; Paniel JB; Gicquel C; Gérard-Blanluet M
    Am J Med Genet A; 2004 Aug; 129A(2):198-200. PubMed ID: 15316976
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.
    Bedeschi MF; Calvello M; Paganini L; Pezzani L; Baccarin M; Fontana L; Sirchia SM; Guerneri S; Canazza L; Leva E; Colombo L; Lalatta F; Mosca F; Tabano S; Miozzo M
    BMC Med Genet; 2017 Oct; 18(1):115. PubMed ID: 29047350
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region.
    Rossignol S; Steunou V; Chalas C; Kerjean A; Rigolet M; Viegas-Pequignot E; Jouannet P; Le Bouc Y; Gicquel C
    J Med Genet; 2006 Dec; 43(12):902-7. PubMed ID: 16825435
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer.
    Chen CP; Su YN; Chen SU; Chang TY; Wu PC; Chern SR; Wu PS; Kuo YL; Wang W
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):90-4. PubMed ID: 24767654
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome.
    Chen CP
    Taiwan J Obstet Gynecol; 2007 Jun; 46(2):96-102. PubMed ID: 17638616
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.
    Gaston V; Le Bouc Y; Soupre V; Burglen L; Donadieu J; Oro H; Audry G; Vazquez MP; Gicquel C
    Eur J Hum Genet; 2001 Jun; 9(6):409-18. PubMed ID: 11436121
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects.
    DeBaun MR; Niemitz EL; McNeil DE; Brandenburg SA; Lee MP; Feinberg AP
    Am J Hum Genet; 2002 Mar; 70(3):604-11. PubMed ID: 11813134
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer.
    Higashimoto K; Soejima H; Saito T; Okumura K; Mukai T
    Cytogenet Genome Res; 2006; 113(1-4):306-12. PubMed ID: 16575194
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A possible relationship between Beckwith-Wiedemann syndrome and prune belly syndrome.
    Silengo M; Barberis L; Ferrero GB; Sorasio L; Valenzise M
    Clin Dysmorphol; 2002 Oct; 11(4):293-4. PubMed ID: 12401997
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndrome.
    Dagar V; Hutchison W; Muscat A; Krishnan A; Hoke D; Buckle A; Siswara P; Amor DJ; Mann J; Pinner J; Colley A; Wilson M; Sachdev R; McGillivray G; Edwards M; Kirk E; Collins F; Jones K; Taylor J; Hayes I; Thompson E; Barnett C; Haan E; Freckmann ML; Turner A; White S; Kamien B; Ma A; Mackenzie F; Baynam G; Kiraly-Borri C; Field M; Dudding-Byth T; Algar EM
    Clin Epigenetics; 2018 Aug; 10(1):114. PubMed ID: 30165906
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome.
    Niemitz EL; DeBaun MR; Fallon J; Murakami K; Kugoh H; Oshimura M; Feinberg AP
    Am J Hum Genet; 2004 Nov; 75(5):844-9. PubMed ID: 15372379
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A possible relationship between Beckwith-Wiedemann syndrome, urinary tract anomaly and prune belly syndrome.
    Watanabe H; Yamanaka T
    Clin Genet; 1990 Dec; 38(6):410-4. PubMed ID: 2289313
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Beckwith-Wiedemann syndrome.
    Choufani S; Shuman C; Weksberg R
    Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):343-54. PubMed ID: 20803657
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.
    Sperandeo MP; Ungaro P; Vernucci M; Pedone PV; Cerrato F; Perone L; Casola S; Cubellis MV; Bruni CB; Andria G; Sebastio G; Riccio A
    Am J Hum Genet; 2000 Mar; 66(3):841-7. PubMed ID: 10712200
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS.
    Bliek J; Maas SM; Ruijter JM; Hennekam RC; Alders M; Westerveld A; Mannens MM
    Hum Mol Genet; 2001 Mar; 10(5):467-76. PubMed ID: 11181570
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS).
    Bliek J; Gicquel C; Maas S; Gaston V; Le Bouc Y; Mannens M
    J Pediatr; 2004 Dec; 145(6):796-9. PubMed ID: 15580204
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Engel JR; Smallwood A; Harper A; Higgins MJ; Oshimura M; Reik W; Schofield PN; Maher ER
    J Med Genet; 2000 Dec; 37(12):921-6. PubMed ID: 11106355
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.
    Arima T; Kamikihara T; Hayashida T; Kato K; Inoue T; Shirayoshi Y; Oshimura M; Soejima H; Mukai T; Wake N
    Nucleic Acids Res; 2005; 33(8):2650-60. PubMed ID: 15888726
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Beckwith-Weidemann syndrome with IC2 (KvDMR1) hypomethylation defect: a novel mutation.
    Pandita A; Gupta S; Gupta G; Panghal A
    BMJ Case Rep; 2018 Mar; 2018():. PubMed ID: 29602885
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Paradoxical NSD1 mutations in Beckwith-Wiedemann syndrome and 11p15 anomalies in Sotos syndrome.
    Baujat G; Rio M; Rossignol S; Sanlaville D; Lyonnet S; Le Merrer M; Munnich A; Gicquel C; Cormier-Daire V; Colleaux L
    Am J Hum Genet; 2004 Apr; 74(4):715-20. PubMed ID: 14997421
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.