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Journal Abstract Search

268 related items for PubMed ID: 7625447

  • 1. Non-random X chromosome inactivation in an affected twin in a monozygotic twin pair discordant for Wiedemann-Beckwith syndrome.
    Orstavik RE, Tommerup N, Eiklid K, Orstavik KH.
    Am J Med Genet; 1995 Mar 27; 56(2):210-4. PubMed ID: 7625447
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  • 2. Monozygotic twinning and Wiedemann-Beckwith syndrome.
    Clayton-Smith J, Read AP, Donnai D.
    Am J Med Genet; 1992 Feb 15; 42(4):633-7. PubMed ID: 1609846
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  • 3. Two pairs of male monozygotic twins discordant for Wiedemann-Beckwith syndrome.
    Leonard NJ, Bernier FP, Rudd N, Machin GA, Bamforth F, Bamforth S, Grundy P, Johnson C.
    Am J Med Genet; 1996 Jan 22; 61(3):253-7. PubMed ID: 8741870
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  • 4. 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 Jan 22; 113(1-4):313-7. PubMed ID: 16575195
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  • 5. Absence of detectable chromosomal and molecular abnormalities in monozygotic twins discordant for the Wiedemann-Beckwith syndrome.
    Litz CE, Taylor KA, Qiu JS, Pescovitz OH, de Martinville B.
    Am J Med Genet; 1988 Jul 22; 30(3):821-33. PubMed ID: 3189402
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  • 7. X-inactivation patterns in monozygotic and dizygotic female twins.
    Goodship J, Carter J, Burn J.
    Am J Med Genet; 1996 Jan 22; 61(3):205-8. PubMed ID: 8741864
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  • 13. X-chromosome inactivation is mostly random in placental tissues of female monozygotic twins and triplets.
    Bamforth F, Machin G, Innes M.
    Am J Med Genet; 1996 Jan 22; 61(3):209-15. PubMed ID: 8741865
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  • 14. X chromosome inactivation patterns correlate with fetal-placental anatomy in monozygotic twin pairs: implications for immune relatedness and concordance for autoimmunity.
    Trejo V, Derom C, Vlietinck R, Ollier W, Silman A, Ebers G, Derom R, Gregersen PK.
    Mol Med; 1994 Nov 22; 1(1):62-70. PubMed ID: 8790602
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  • 16. Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.
    Kubota T, Saitoh S, Matsumoto T, Narahara K, Fukushima Y, Jinno Y, Niikawa N.
    Am J Med Genet; 1994 Feb 15; 49(4):378-83. PubMed ID: 7909196
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