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Journal Abstract Search

216 related items for PubMed ID: 8968740

  • 21. Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.
    Wu YQ, Sutton VR, Nickerson E, Lupski JR, Potocki L, Korenberg JR, Greenberg F, Tassabehji M, Shaffer LG.
    Am J Med Genet; 1998 Jun 16; 78(1):82-9. PubMed ID: 9637430
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  • 22. Williams-Beuren syndrome: unraveling the mysteries of a microdeletion disorder.
    Osborne LR.
    Mol Genet Metab; 1999 May 16; 67(1):1-10. PubMed ID: 10329018
    [No Abstract] [Full Text] [Related]

  • 23. Mutational mechanisms of Williams-Beuren syndrome deletions.
    Bayés M, Magano LF, Rivera N, Flores R, Pérez Jurado LA.
    Am J Hum Genet; 2003 Jul 16; 73(1):131-51. PubMed ID: 12796854
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  • 24. Atypical 7q11.23 deletions excluding ELN gene result in Williams-Beuren syndrome craniofacial features and neurocognitive profile.
    Alesi V, Loddo S, Orlando V, Genovese S, Di Tommaso S, Liambo MT, Pompili D, Ferretti D, Calacci C, Catino G, Falasca R, Dentici ML, Novelli A, Digilio MC, Dallapiccola B.
    Am J Med Genet A; 2021 Jan 16; 185(1):242-249. PubMed ID: 33098373
    [Abstract] [Full Text] [Related]

  • 25. FISH analysis in patients with clinical diagnosis of Williams syndrome.
    Elçioglu N, Mackie-Ogilvie C, Daker M, Berry AC.
    Acta Paediatr; 1998 Jan 16; 87(1):48-53. PubMed ID: 9510447
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  • 28. A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.
    Osborne LR, Li M, Pober B, Chitayat D, Bodurtha J, Mandel A, Costa T, Grebe T, Cox S, Tsui LC, Scherer SW.
    Nat Genet; 2001 Nov 16; 29(3):321-5. PubMed ID: 11685205
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  • 29. Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers.
    Dutra RL, Pieri Pde C, Teixeira AC, Honjo RS, Bertola DR, Kim CA.
    Clinics (Sao Paulo); 2011 Nov 16; 66(6):959-64. PubMed ID: 21808859
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  • 31. Copy number variants at Williams-Beuren syndrome 7q11.23 region.
    Merla G, Brunetti-Pierri N, Micale L, Fusco C.
    Hum Genet; 2010 Jul 16; 128(1):3-26. PubMed ID: 20437059
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  • 32. Williams-Beuren syndrome: a model of recurrent genomic mutation.
    Pérez Jurado AL.
    Horm Res; 2003 Jul 16; 59 Suppl 1():106-13. PubMed ID: 12638521
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  • 35. [Genetic diagnosis of Williams syndrome].
    Urbán Z, Kiss E, Kádár K, Szabolcs J, Csiszár K, Boyd DC, Fekete G.
    Orv Hetil; 1997 Jul 06; 138(27):1749-52. PubMed ID: 9273487
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  • 36. Elastin region deletions in Williams syndrome.
    Zhang J, Kumar A, Roux K, Williams CA, Wallace MR.
    Genet Test; 1999 Jul 06; 3(4):357-9. PubMed ID: 10627943
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  • 38. Clinical and molecular cytogenetic (FISH) diagnosis of Williams syndrome.
    Brewer CM, Morrison N, Tolmie JL.
    Arch Dis Child; 1996 Jan 06; 74(1):59-61. PubMed ID: 8660051
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