BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 19474816)

  • 21. New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome.
    Smith AC; Rubin T; Shuman C; Estabrooks L; Aylsworth AS; McDonald MT; Steele L; Ray PN; Weksberg R
    Cytogenet Genome Res; 2006; 113(1-4):313-7. PubMed ID: 16575195
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Wiedemann-Beckwith syndrome: further prenatal characterization of the condition.
    Reish O; Lerer I; Amiel A; Heyman E; Herman A; Dolfin T; Abeliovich D
    Am J Med Genet; 2002 Jan; 107(3):209-13. PubMed ID: 11807901
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndrome.
    Smith AC; Squire JA; Thorner P; Zielenska M; Shuman C; Grant R; Chitayat D; Nishikawa JL; Weksberg R
    Pediatr Dev Pathol; 2001; 4(6):550-8. PubMed ID: 11826361
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Metastatic Phyllodes Tumor in a Patient With Beckwith-Wiedemann Syndrome.
    Saini A; Gupte T; Choudhury MSR; Jacques SM; Roxas R
    J Investig Med High Impact Case Rep; 2022; 10():23247096221133197. PubMed ID: 36314358
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Chest wall hamartoma with Wiedemann-Beckwith syndrome: clinical report and brief review of chromosome 11p15.5-related tumors.
    Jonas RE; Kimonis VE
    Am J Med Genet; 2001 Jul; 101(3):221-5. PubMed ID: 11424137
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.
    Soejima H; Higashimoto K
    J Hum Genet; 2013 Jul; 58(7):402-9. PubMed ID: 23719190
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal detection of a congenital pancreatic cyst and Beckwith-Wiedemann syndrome.
    Fremond B; Poulain P; Odent S; Milon J; Treguier C; Babut JM
    Prenat Diagn; 1997 Mar; 17(3):276-80. PubMed ID: 9110373
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 11p15 duplication and 13q34 deletion with Beckwith-Wiedemann syndrome and factor VII deficiency.
    Jurkiewicz D; Kugaudo M; Tańska A; Wawrzkiewicz-Witkowska A; Tomaszewska A; Kucharczyk M; Cieślikowska A; Ciara E; Krajewska-Walasek M
    Pediatr Int; 2015 Jun; 57(3):486-91. PubMed ID: 26012727
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Pediatric Cushing syndrome: An early sign of an underling cancer predisposition syndrome.
    Schweiger BM; Esakhan CL; Frishberg D; Grand K; Garg R; Sanchez-Lara PA
    Am J Med Genet A; 2021 Sep; 185(9):2824-2828. PubMed ID: 33960620
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Bilateral cystic adrenal masses in the neonate associated with the incomplete form of Beckwith-Wiedemann syndrome.
    Akata D; Haliloğlu M; Ozmen MN; Akhan O
    Pediatr Radiol; 1997 Jan; 27(1):1-2. PubMed ID: 8995155
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Familial Beckwith-Wiedemann syndrome: Prenatal manifestation and a possible expansion of the phenotype.
    Brabbing-Goldstein D; Yaron Y; Reches A
    Eur J Med Genet; 2021 Feb; 64(2):104137. PubMed ID: 33421606
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Wiedemann-Beckwith syndrome with congenital central hypothyroidism in one of monozygotic twins.
    Chien CH; Lee JS; Tsai WY; Wang TR
    J Formos Med Assoc; 1990 Feb; 89(2):132-6. PubMed ID: 1973721
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hypoglycemia in Beckwith-Wiedemann syndrome.
    DeBaun MR; King AA; White N
    Semin Perinatol; 2000 Apr; 24(2):164-71. PubMed ID: 10805171
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidism.
    Martínez y Martínez R; Ocampo-Campos R; Pérez-Arroyo R; Corona-Rivera E; Cantú JM
    Eur J Pediatr; 1985 Jan; 143(3):233-5. PubMed ID: 3987723
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe.
    Barisic I; Boban L; Akhmedzhanova D; Bergman JEH; Cavero-Carbonell C; Grinfelde I; Materna-Kiryluk A; Latos-Bieleńska A; Randrianaivo H; Zymak-Zakutnya N; Sansovic I; Lanzoni M; Morris JK
    Eur J Med Genet; 2018 Sep; 61(9):499-507. PubMed ID: 29753922
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Beckwith-Wiedemann syndrome with placental chorangioma due to H19-differentially methylated region hypermethylation: a case report.
    Aoki A; Shiozaki A; Sameshima A; Higashimoto K; Soejima H; Saito S
    J Obstet Gynaecol Res; 2011 Dec; 37(12):1872-6. PubMed ID: 21955307
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Beckwith-Wiedemann Syndrome (BWS): a case report and literature review.
    Ogundiran TO; Aghahowa ME; Brown BJ; Irabor DO
    West Afr J Med; 2003; 22(1):101-2. PubMed ID: 12769320
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal sonographic diagnosis of Beckwith-Wiedemann syndrome in association with a single umbilical artery.
    Hamada H; Fujiki Y; Obata-Yasuoka M; Watanabe H; Yamada N; Kubo T
    J Clin Ultrasound; 2001; 29(9):535-8. PubMed ID: 11745867
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Beckwith-Wiedemann-like macroglossia and 18q23 haploinsufficiency.
    Lirussi F; Jonard L; Gaston V; Sanlaville D; Kooy RF; Winnepenninckx B; Maher ER; Fitzpatrick DR; Gicquel C; Portnoï MF; Couderc R; Vazquez MP; Bahuau M
    Am J Med Genet A; 2007 Dec; 143A(23):2796-803. PubMed ID: 17994567
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.