These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 2309794)

  • 21. Pancreatoblastoma associated with incomplete Beckwith-Wiedemann syndrome: case report and review of the literature.
    Muguerza R; Rodriguez A; Formigo E; Montero M; Vázquez JL; Páramo C; Campos C
    J Pediatr Surg; 2005 Aug; 40(8):1341-4. PubMed ID: 16080945
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular biology of Beckwith-Wiedemann syndrome.
    Weksberg R; Squire JA
    Med Pediatr Oncol; 1996 Nov; 27(5):462-9. PubMed ID: 8827075
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Mediastinal neuroblastoma in Wiedemann-Beckwith syndrome].
    Huber A; Gutjahr P
    Monatsschr Kinderheilkd; 1989 Apr; 137(4):243-4. PubMed ID: 2733702
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Nonmalignant renal disease in pediatric patients with Beckwith-Wiedemann syndrome.
    Choyke PL; Siegel MJ; Oz O; Sotelo-Avila C; DeBaun MR
    AJR Am J Roentgenol; 1998 Sep; 171(3):733-7. PubMed ID: 9725306
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Simultaneous occurrence of pancreatoblastoma and neuroblastoma in a newborn with beckwith-wiedemann syndrome.
    Sorrentino S; Conte M; Nozza P; Granata C; Capra V; Avanzini S; Garaventa A
    J Pediatr Hematol Oncol; 2010 Jul; 32(5):e207-9. PubMed ID: 20495482
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG
    Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Acute megakaryocytic leukemia (AMKL,FAB;M7) with Beckwith-Wiedemann syndrome.
    Yamamoto S; Toyama D; Yatsuki H; Higashimoto K; Soejima H; Isoyama K
    Pediatr Blood Cancer; 2010 Oct; 55(4):733-5. PubMed ID: 20589645
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Follow-up study of patients with Wiedemann-Beckwith syndrome with emphasis on the change in facial appearance over time.
    Hunter AG; Allanson JE
    Am J Med Genet; 1994 Jun; 51(2):102-7. PubMed ID: 8092184
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Neuroblastoma in a patient with the Beckwith-Wiedemann syndrome (BWS).
    Yoon G; Graham G; Weksberg R; Gaul HP; DeBaun MR; Coppes MJ
    Med Pediatr Oncol; 2002 Mar; 38(3):193-9. PubMed ID: 11836721
    [No Abstract]   [Full Text] [Related]  

  • 30. Genetic factors in solid tumors of childhood.
    Ponz de Leon M
    Recent Results Cancer Res; 1994; 136():48-58. PubMed ID: 7863106
    [No Abstract]   [Full Text] [Related]  

  • 31. 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]  

  • 32. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.
    Hatada I; Ohashi H; Fukushima Y; Kaneko Y; Inoue M; Komoto Y; Okada A; Ohishi S; Nabetani A; Morisaki H; Nakayama M; Niikawa N; Mukai T
    Nat Genet; 1996 Oct; 14(2):171-3. PubMed ID: 8841187
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-beckwith syndrome.
    Itoh N; Becroft DM; Reeve AE; Morison IM
    Am J Med Genet; 2000 May; 92(2):111-6. PubMed ID: 10797434
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Beckwith-Wiedemann syndrome.
    Weksberg R; Shuman C; Smith AC
    Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):12-23. PubMed ID: 16010676
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.
    Riccio A; Sparago A; Verde G; De Crescenzo A; Citro V; Cubellis MV; Ferrero GB; Silengo MC; Russo S; Larizza L; Cerrato F
    Endocr Dev; 2009; 14():1-9. PubMed ID: 19293570
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor.
    Prawitt D; Enklaar T; Gärtner-Rupprecht B; Spangenberg C; Lausch E; Reutzel D; Fees S; Korzon M; Brozek I; Limon J; Housman DE; Pelletier J; Zabel B
    Nat Genet; 2005 Aug; 37(8):785-6; author reply 786-7. PubMed ID: 16049499
    [No Abstract]   [Full Text] [Related]  

  • 38. Renal findings on radiological followup of patients with Beckwith-Wiedemann syndrome.
    Borer JG; Kaefer M; Barnewolt CE; Elias ER; Hobbs N; Retik AB; Peters CA
    J Urol; 1999 Jan; 161(1):235-9. PubMed ID: 10037413
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Simultaneous occurrence of right adrenocortical tumor and left adrenal neuroblastoma in an infant with Beckwith-Wiedemann syndrome.
    Alsultan A; Lovell MA; Hayes KL; Allshouse MJ; Garrington TP
    Pediatr Blood Cancer; 2008 Nov; 51(5):695-8. PubMed ID: 18668518
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Familial posterior helical ear pits and Wiedemann-Beckwith syndrome.
    Best LG
    Am J Med Genet; 1991 Aug; 40(2):188-95. PubMed ID: 1897573
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.