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Journal Abstract Search


175 related items for PubMed ID: 8741870

  • 21. Monozygotic twins discordant for vascular malformations and dysregulated growth.
    Oduber CE, Bliek J, van der Horst CM, van Steensel MA, Hennekam RC.
    Eur J Med Genet; 2010; 53(1):14-8. PubMed ID: 19716450
    [Abstract] [Full Text] [Related]

  • 22. (Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith-Wiedemann syndrome.
    Fontana L, Bedeschi MF, Cagnoli GA, Costanza J, Persico N, Gangi S, Porro M, Ajmone PF, Colapietro P, Santaniello C, Crippa M, Sirchia SM, Miozzo M, Tabano S.
    Mol Genet Genomic Med; 2020 Sep; 8(9):e1386. PubMed ID: 32627967
    [Abstract] [Full Text] [Related]

  • 23. Monozygotic twinning and Wiedemann-Beckwith syndrome.
    Franceschini P, Guala A, Vardeu MP, Franceschini D.
    Am J Med Genet; 1993 May 15; 46(3):353-4. PubMed ID: 8488888
    [No Abstract] [Full Text] [Related]

  • 24. 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 15; 146(4):565-7. PubMed ID: 15812468
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  • 26. Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
    Fryns JP, Kleczkowska A, Devriendt K, Devliegher H, Van den Berghe H.
    Genet Couns; 1993 Apr 15; 4(1):37-41. PubMed ID: 8471219
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  • 27. Beckwith-Wiedemann syndrome: multiple molecular mechanisms.
    Enklaar T, Zabel BU, Prawitt D.
    Expert Rev Mol Med; 2006 Jul 17; 8(17):1-19. PubMed ID: 16842655
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  • 29. [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 17; 91(11):837-40. PubMed ID: 16264244
    [Abstract] [Full Text] [Related]

  • 30. Diagnosis and management of the phenotypic spectrum of twins with Beckwith-Wiedemann syndrome.
    Cohen JL, Duffy KA, Sajorda BJ, Hathaway ER, Gonzalez-Gandolfi CX, Richards-Yutz J, Gunter AT, Ganguly A, Kaplan J, Deardorff MA, Kalish JM.
    Am J Med Genet A; 2019 Jul 17; 179(7):1139-1147. PubMed ID: 31067005
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  • 31. The prenatal diagnosis of Beckwith-Wiedemann syndrome using ultrasound and magnetic resonance imaging.
    Storm DW, Hirselj DA, Rink B, O'Shaughnessy R, Alpert SA.
    Urology; 2011 Jan 17; 77(1):208-10. PubMed ID: 20573391
    [Abstract] [Full Text] [Related]

  • 32. Imprinting errors and developmental asymmetry.
    Bestor TH.
    Philos Trans R Soc Lond B Biol Sci; 2003 Aug 29; 358(1436):1411-5. PubMed ID: 14511489
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  • 33. First report on concordant monozygotic twins with Silver-Russell syndrome and ICR1 hypomethylation.
    Riess A, Binder G, Ziegler J, Begemann M, Soellner L, Eggermann T.
    Eur J Med Genet; 2016 Jan 29; 59(1):1-4. PubMed ID: 26691664
    [Abstract] [Full Text] [Related]

  • 34. A child with Beckwith-Wiedemann syndrome and posterior urethral valves.
    Buyukcelik M, Satar N, Dursun H, Bayazit Y, Bayazit AK, Soran M, Noyan A, Anarat A.
    Genet Couns; 2005 Jan 29; 16(1):41-4. PubMed ID: 15844777
    [Abstract] [Full Text] [Related]

  • 35. Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family.
    Best LG, Hoekstra RE.
    Am J Med Genet; 1981 Jan 29; 9(4):291-9. PubMed ID: 7294068
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  • 36. Tongue reduction in Beckwith-Wiedemann syndrome with CO(2) laser.
    Yilmaz M, Mercan H, Karaman E, Kaytaz A.
    J Craniofac Surg; 2009 Jul 29; 20(4):1202-3. PubMed ID: 19553838
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  • 38. Monozygotic twins clinically discordant for scleroderma show concordance for fibroblast gene expression profiles.
    Zhou X, Tan FK, Xiong M, Arnett FC, Feghali-Bostwick CA.
    Arthritis Rheum; 2005 Oct 29; 52(10):3305-14. PubMed ID: 16200604
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  • 39. [Wiedemann-Beckwith syndrome: clinical and epidemiological analysis of a consecutive series of cases in Spain].
    Arroyo Carrera I, Martínez-Frías ML, Egüés Jimeno J, García Martínez MJ, Eloína Cimadevilla Sánchez C, Bermejo Sánchez E.
    An Esp Pediatr; 1999 Feb 29; 50(2):161-5. PubMed ID: 10199027
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  • 40. Congenital stapedial fixation associated with Beckwith--Wiedemann syndrome: two cases of a woman and her brother.
    Takahashi S, Shinoda H, Nakano Y.
    Am J Otol; 1996 Jan 29; 17(1):111-4. PubMed ID: 8694112
    [Abstract] [Full Text] [Related]


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