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Journal Abstract Search

169 related items for PubMed ID: 10720981

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  • 7. FISH analysis in patients with clinical diagnosis of Williams syndrome.
    Elçioglu N, Mackie-Ogilvie C, Daker M, Berry AC.
    Acta Paediatr; 1998 Jan; 87(1):48-53. PubMed ID: 9510447
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  • 8. Elastin gene deletions in Williams syndrome.
    Smoot LB.
    Curr Opin Pediatr; 1995 Dec; 7(6):698-701. PubMed ID: 8776022
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  • 15. Clinical and molecular cytogenetic (FISH) diagnosis of Williams syndrome.
    Brewer CM, Morrison N, Tolmie JL.
    Arch Dis Child; 1996 Jan; 74(1):59-61. PubMed ID: 8660051
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  • 16. Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome.
    Mari A, Amati F, Mingarelli R, Giannotti A, Sebastio G, Colloridi V, Novelli G, Dallapiccola B.
    Hum Genet; 1995 Oct; 96(4):444-8. PubMed ID: 7557968
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  • 17. 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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  • 18. A Case Report of in Utero Williams Syndrome Arterial Malformation.
    Kobalka AJ, Mrak RE, Gunning WT.
    Fetal Pediatr Pathol; 2017 Dec 16; 36(6):452-456. PubMed ID: 29227713
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  • 20. The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome.
    Duba HC, Doll A, Neyer M, Erdel M, Mann C, Hammerer I, Utermann G, Grzeschik KH.
    Eur J Hum Genet; 2002 Jun 16; 10(6):351-61. PubMed ID: 12080386
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