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Journal Abstract Search

179 related items for PubMed ID: 10486217

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  • 3. 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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  • 4. Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome.
    Wang YK, Spörle R, Paperna T, Schughart K, Francke U.
    Genomics; 1999 Apr 15; 57(2):235-48. PubMed ID: 10198163
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  • 5. Mapping of the human HPC-1/syntaxin 1A gene (STX1A) to chromosome 7 band q11.2.
    Nakayama T, Fujiwara T, Miyazawa A, Asakawa S, Shimizu N, Shimizu Y, Mikoshiba K, Akagawa K.
    Genomics; 1997 May 15; 42(1):173-6. PubMed ID: 9177791
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  • 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
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  • 7. 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 15; 8(3):215-22. PubMed ID: 10780788
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  • 8. 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 15; 10(6):351-61. PubMed ID: 12080386
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  • 9. Zebrafish gene knockdowns imply roles for human YWHAG in infantile spasms and cardiomegaly.
    Komoike Y, Fujii K, Nishimura A, Hiraki Y, Hayashidani M, Shimojima K, Nishizawa T, Higashi K, Yasukawa K, Saitsu H, Miyake N, Mizuguchi T, Matsumoto N, Osawa M, Kohno Y, Higashinakagawa T, Yamamoto T.
    Genesis; 2010 Apr 15; 48(4):233-43. PubMed ID: 20146355
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  • 10. 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
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  • 11. Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome.
    Tipney HJ, Hinsley TA, Brass A, Metcalfe K, Donnai D, Tassabehji M.
    Eur J Hum Genet; 2004 Jul 01; 12(7):551-60. PubMed ID: 15100712
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  • 12. Molecular cloning and characterization of a novel human CC chemokine, SCYA26.
    Guo RF, Ward PA, Hu SM, McDuffie JE, Huber-Lang M, Shi MM.
    Genomics; 1999 Jun 15; 58(3):313-7. PubMed ID: 10373330
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  • 16. A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome.
    Tassabehji M, Carette M, Wilmot C, Donnai D, Read AP, Metcalfe K.
    Eur J Hum Genet; 1999 Jun 15; 7(7):737-47. PubMed ID: 10573005
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  • 17. Molecular cloning, expression and chromosomal localization of a novel human REG family gene, REG III.
    Nata K, Liu Y, Xu L, Ikeda T, Akiyama T, Noguchi N, Kawaguchi S, Yamauchi A, Takahashi I, Shervani NJ, Onogawa T, Takasawa S, Okamoto H.
    Gene; 2004 Sep 29; 340(1):161-70. PubMed ID: 15556304
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  • 18. Mapping of the human cysteine-rich intestinal protein gene CRIP1 to the human chromosomal segment 7q11.23.
    Garcia-Barcelo M, Tsui SK, Chim SS, Fung KP, Lee CY, Waye MM.
    Genomics; 1998 Feb 01; 47(3):419-22. PubMed ID: 9480758
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  • 19. Cloning, structural organization analysis, and chromosomal assignment of the human gene for the neurosecretory protein VGF.
    Canu N, Possenti R, Ricco AS, Rocchi M, Levi A.
    Genomics; 1997 Oct 15; 45(2):443-6. PubMed ID: 9344675
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