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Journal Abstract Search

177 related items for PubMed ID: 8812460

  • 1. Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients.
    Osborne LR, Martindale D, Scherer SW, Shi XM, Huizenga J, Heng HH, Costa T, Pober B, Lew L, Brinkman J, Rommens J, Koop B, Tsui LC.
    Genomics; 1996 Sep 01; 36(2):328-36. PubMed ID: 8812460
    [Abstract] [Full Text] [Related]

  • 2. 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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  • 3. 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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  • 4. 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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  • 5. A novel human gene, WSTF, is deleted in Williams syndrome.
    Lu X, Meng X, Morris CA, Keating MT.
    Genomics; 1998 Dec 01; 54(2):241-9. PubMed ID: 9828126
    [Abstract] [Full Text] [Related]

  • 6. Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome.
    Osborne LR, Campbell T, Daradich A, Scherer SW, Tsui LC.
    Genomics; 1999 Apr 15; 57(2):279-84. PubMed ID: 10198167
    [Abstract] [Full Text] [Related]

  • 7. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).
    Valero MC, de Luis O, Cruces J, Pérez Jurado LA.
    Genomics; 2000 Oct 01; 69(1):1-13. PubMed ID: 11013070
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  • 10. Autism and Williams syndrome: a case report.
    Herguner S, Mukaddes NM.
    World J Biol Psychiatry; 2006 Oct 01; 7(3):186-8. PubMed ID: 16861145
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  • 14. In-depth analysis of spatial cognition in Williams syndrome: A critical assessment of the role of the LIMK1 gene.
    Gray V, Karmiloff-Smith A, Funnell E, Tassabehji M.
    Neuropsychologia; 2006 Oct 01; 44(5):679-85. PubMed ID: 16216290
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  • 15. Identification of additional transcripts in the Williams-Beuren syndrome critical region.
    Merla G, Ucla C, Guipponi M, Reymond A.
    Hum Genet; 2002 May 01; 110(5):429-38. PubMed ID: 12073013
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  • 16. [Williams syndrome without cardiovascular abnormalities].
    Cincinnati P, Genuardi M, Rutiloni C.
    Minerva Pediatr; 1998 Nov 01; 50(11):467-71. PubMed ID: 10207296
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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. Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.
    Mizugishi K, Yamanaka K, Kuwajima K, Kondo I.
    J Hum Genet; 1998 Jun 16; 43(3):178-81. PubMed ID: 9747030
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  • 19. Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion.
    Robinson WP, Waslynka J, Bernasconi F, Wang M, Clark S, Kotzot D, Schinzel A.
    Genomics; 1996 May 15; 34(1):17-23. PubMed ID: 8661020
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