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Journal Abstract Search

197 related items for PubMed ID: 10207296

  • 1. [Williams syndrome without cardiovascular abnormalities].
    Cincinnati P, Genuardi M, Rutiloni C.
    Minerva Pediatr; 1998 Nov; 50(11):467-71. PubMed ID: 10207296
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  • 2. Autism and Williams syndrome: a case report.
    Herguner S, Mukaddes NM.
    World J Biol Psychiatry; 2006 Nov; 7(3):186-8. PubMed ID: 16861145
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  • 3. [Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome].
    Milà M, Carrió A, Sánchez A, Gómez D, Jiménez D, Estivill X, Ballesta F.
    Med Clin (Barc); 1999 Jun 19; 113(2):46-9. PubMed ID: 10425618
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  • 12. A complete physical contig and partial transcript map of the Williams syndrome critical region.
    Hockenhull EL, Carette MJ, Metcalfe K, Donnai D, Read AP, Tassabehji M.
    Genomics; 1999 Jun 01; 58(2):138-45. PubMed ID: 10366445
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  • 13. WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog.
    de Luis O, Valero MC, Jurado LA.
    Eur J Hum Genet; 2000 Mar 01; 8(3):215-22. PubMed ID: 10780788
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  • 14. MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams-Beuren syndrome regions.
    Kirchhoff M, Bisgaard AM, Bryndorf T, Gerdes T.
    Eur J Med Genet; 2007 Mar 01; 50(1):33-42. PubMed ID: 17090394
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  • 15. A novel human gene FKBP6 is deleted in Williams syndrome.
    Meng X, Lu X, Morris CA, Keating MT.
    Genomics; 1998 Sep 01; 52(2):130-7. PubMed ID: 9782077
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  • 16. Infantile spasms in two children with Williams syndrome.
    Tsao CY, Westman JA.
    Am J Med Genet; 1997 Jul 11; 71(1):54-6. PubMed ID: 9215769
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  • 19. Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.
    Van der Aa N, Rooms L, Vandeweyer G, van den Ende J, Reyniers E, Fichera M, Romano C, Delle Chiaie B, Mortier G, Menten B, Destrée A, Maystadt I, Männik K, Kurg A, Reimand T, McMullan D, Oley C, Brueton L, Bongers EM, van Bon BW, Pfund R, Jacquemont S, Ferrarini A, Martinet D, Schrander-Stumpel C, Stegmann AP, Frints SG, de Vries BB, Ceulemans B, Kooy RF.
    Eur J Med Genet; 2009 Jul 11; 52(2-3):94-100. PubMed ID: 19249392
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  • 20. Williams syndrome and the elastin gene in Thai patients.
    Ruangdaraganon N, Tocharoentanaphol C, Kotchabhakdi N, Khowsathit P.
    J Med Assoc Thai; 1999 Nov 11; 82 Suppl 1():S174-8. PubMed ID: 10730539
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