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Journal Abstract Search

219 related items for PubMed ID: 10987657

  • 1. Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome.
    Joyce CA, Sharp A, Walker JM, Bullman H, Temple IK.
    Hum Genet; 1999 Sep; 105(3):273-80. PubMed ID: 10987657
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  • 2. Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome.
    Monk D, Wakeling EL, Proud V, Hitchins M, Abu-Amero SN, Stanier P, Preece MA, Moore GE.
    Am J Hum Genet; 2000 Jan; 66(1):36-46. PubMed ID: 10631135
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  • 3. Gene dosage analysis in Silver-Russell syndrome: use of quantitative competitive PCR and dual-color FISH to estimate the frequency of duplications in 7p11.2-p13.
    Mergenthaler S, Sharp A, Ranke MB, Kalscheuer VM, Wollmann HA, Eggermann T.
    Genet Test; 2001 Jan; 5(3):261-6. PubMed ID: 11788094
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  • 4. Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome.
    Hitchins MP, Monk D, Bell GM, Ali Z, Preece MA, Stanier P, Moore GE.
    Eur J Hum Genet; 2001 Feb; 9(2):82-90. PubMed ID: 11313740
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  • 5. DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed.
    Hitchins MP, Bentley L, Monk D, Beechey C, Peters J, Kelsey G, Ishino F, Preece MA, Stanier P, Moore GE.
    Mamm Genome; 2002 Dec; 13(12):686-91. PubMed ID: 12514746
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  • 6. Heterogeneous growth patterns in carriers of chromosome 7p12.2 imbalances affecting GRB10.
    Eggermann T, Begemann M, Gogiel M, Palomares M, Vallespín E, Fernández L, Cazorla R, Spengler S, García-Miñaúr S.
    Am J Med Genet A; 2012 Nov; 158A(11):2815-9. PubMed ID: 22987336
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  • 8. Recombinant Chromosome 7 Driven by Maternal Chromosome 7 Pericentric Inversion in a Girl with Features of Silver-Russell Syndrome.
    Catusi I, Bonati MT, Mainini E, Russo S, Orlandini E, Larizza L, Recalcati MP.
    Int J Mol Sci; 2020 Nov 11; 21(22):. PubMed ID: 33187293
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  • 9. Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely.
    Eggermann K, Wollmann HA, Binder G, Kaiser P, Ranke MB, Eggermann T.
    Ann Genet; 1999 Nov 11; 42(2):117-21. PubMed ID: 10434128
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  • 13. Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene.
    Miyoshi N, Kuroiwa Y, Kohda T, Shitara H, Yonekawa H, Kawabe T, Hasegawa H, Barton SC, Surani MA, Kaneko-Ishino T, Ishino F.
    Proc Natl Acad Sci U S A; 1998 Feb 03; 95(3):1102-7. PubMed ID: 9448292
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  • 14. Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.
    Monk D, Bentley L, Hitchins M, Myler RA, Clayton-Smith J, Ismail S, Price SM, Preece MA, Stanier P, Moore GE.
    Hum Genet; 2002 Oct 03; 111(4-5):376-87. PubMed ID: 12384779
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  • 15. Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variations.
    Eggermann T, Begemann M, Kurth I, Elbracht M.
    Eur J Med Genet; 2019 Jul 03; 62(7):103671. PubMed ID: 31100449
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  • 16. Silver-Russell syndrome due to maternal uniparental disomy 7 and a familial reciprocal translocation t(7;13).
    Behnecke A, Hinderhofer K, Jauch A, Janssen JW, Moog U.
    Clin Genet; 2012 Nov 03; 82(5):494-8. PubMed ID: 21954990
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  • 17. Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis.
    Monk D, Smith R, Arnaud P, Preece MA, Stanier P, Beechey CV, Peters J, Kelsey G, Moore GE.
    Mamm Genome; 2003 Dec 03; 14(12):805-16. PubMed ID: 14724735
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  • 18. Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome.
    Yoshihashi H, Maeyama K, Kosaki R, Ogata T, Tsukahara M, Goto Y, Hata J, Matsuo N, Smith RJ, Kosaki K.
    Am J Hum Genet; 2000 Aug 03; 67(2):476-82. PubMed ID: 10856193
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  • 19. Maternal heterodisomy/isodisomy and paternal supernumerary ring of chromosome 7 in a child with Silver-Russell syndrome.
    Combi R, Sala E, Villa N, Crosti F, Beccaria L, Cogliardi A, Tenchini ML, Dalprà L.
    Clin Dysmorphol; 2008 Jan 03; 17(1):35-39. PubMed ID: 18049079
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