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 *

184 related articles for article (PubMed ID: 4091589)

  • 21. Imprinting errors and developmental asymmetry.
    Bestor TH
    Philos Trans R Soc Lond B Biol Sci; 2003 Aug; 358(1436):1411-5. PubMed ID: 14511489
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Twin-twin transfusion resulting in fetal cell contamination in Beckwith-Wiedemann syndrome.
    Zarate YA; Hopkin RJ
    Am J Med Genet A; 2009 Jul; 149A(7):1569-70. PubMed ID: 19533777
    [No Abstract]   [Full Text] [Related]  

  • 23. Dizygotic twin pregnancy conceived with assisted reproductive technology associated with chromosomal anomaly, imprinting disorder, and monochorionic placentation.
    Yoon G; Beischel LS; Johnson JP; Jones MC
    J Pediatr; 2005 Apr; 146(4):565-7. PubMed ID: 15812468
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Esophageal atresia and Beckwith-Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first report.
    Serra G; Antona V; Schierz M; Vecchio D; Piro E; Corsello G
    Clin Case Rep; 2018 Feb; 6(2):399-401. PubMed ID: 29445485
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [The Wiedemann-Beckwith syndrome and a congenital cataract].
    Momtchilova M; Pelosse B; Laroche L; Vazquez MP
    J Fr Ophtalmol; 2001 May; 24(5):479-81. PubMed ID: 11397983
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Discordant expression of the G syndrome in monozygotic twins.
    Young ID; Dalgleish R; MacKay EH; MacFadyen UM
    Am J Med Genet; 1988 Apr; 29(4):863-9. PubMed ID: 3400731
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Continuous hypomethylation of the KCNQ1OT1:TSS-DMR in monochorionic twins discordant for Beckwith-Wiedemann syndrome.
    Inoue T; Nakamura A; Matsubara K; Nyuzuki H; Nagasaki K; Oka A; Fukami M; Kagami M
    Am J Med Genet A; 2017 Oct; 173(10):2847-2850. PubMed ID: 28816024
    [No Abstract]   [Full Text] [Related]  

  • 29. Beckwith-Wiedemann syndrome, tumourigenesis and imprinting.
    Junien C
    Curr Opin Genet Dev; 1992 Jun; 2(3):431-8. PubMed ID: 1504618
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The de Lange syndrome in one of twins.
    Carakushannsky G; Berthier C
    J Med Genet; 1976 Oct; 13(5):404-6. PubMed ID: 1034016
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Isolated fetal omphalocele, Beckwith-Wiedemann syndrome, and assisted reproductive technologies.
    Wilkins-Haug L; Porter A; Hawley P; Benson CB
    Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):58-62. PubMed ID: 19107956
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Premature infant with Wiedemann-Beckwith syndrome: postnatal changes in facial appearance and somatic phenotype.
    Stratakis CA; Garnica A
    Am J Med Genet; 1995 Jul; 57(4):635-6. PubMed ID: 7573144
    [No Abstract]   [Full Text] [Related]  

  • 33. 45,X/46,XX mosaicism in discordant monozygotic twins.
    Uchida IA; deSa DJ; Whelan DT
    Pediatrics; 1983 Mar; 71(3):413-7. PubMed ID: 6572357
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Beckwith-Wiedemann syndrome. An update and review for the primary pediatrician.
    Weng EY; Mortier GR; Graham JM
    Clin Pediatr (Phila); 1995 Jun; 34(6):317-26. PubMed ID: 7656512
    [No Abstract]   [Full Text] [Related]  

  • 35. [Uniparental disomy of chromosome 11 in a patient with Beckwith-Wiedemann syndrome. First reported case in Iceland].
    Pálsson GI; Finnsdóttir V; Jóhannsson JH; Ingvarsson S
    Laeknabladid; 2005 Nov; 91(11):837-40. PubMed ID: 16264244
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [The Wiedemann-Beckwith syndrome. Its natural history and levels of prevention].
    Martínez y Martínez R; Martínez-Carboney R
    Gac Med Mex; 1997; 133(3):195-202. PubMed ID: 9303867
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. 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]  

  • 40. Monozygotic twins discordant for trisomy 13.
    Ramsey KW; Slavin TP; Graham G; Hirata GI; Balaraman V; Seaver LH
    J Perinatol; 2012 Apr; 32(4):306-8. PubMed ID: 22460600
    [TBL] [Abstract][Full Text] [Related]  

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