BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

271 related articles for article (PubMed ID: 12073013)

  • 1. Identification of additional transcripts in the Williams-Beuren syndrome critical region.
    Merla G; Ucla C; Guipponi M; Reymond A
    Hum Genet; 2002 May; 110(5):429-38. PubMed ID: 12073013
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 57(2):279-84. PubMed ID: 10198167
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 69(1):1-13. PubMed ID: 11013070
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 12(7):551-60. PubMed ID: 15100712
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome.
    Doll A; Grzeschik KH
    Cytogenet Cell Genet; 2001; 95(1-2):20-7. PubMed ID: 11978965
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 8(3):215-22. PubMed ID: 10780788
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel human gene FKBP6 is deleted in Williams syndrome.
    Meng X; Lu X; Morris CA; Keating MT
    Genomics; 1998 Sep; 52(2):130-7. PubMed ID: 9782077
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Williams-Beuren syndrome: determination of deletion size using quantitative real-time PCR.
    Schubert C; Laccone F
    Int J Mol Med; 2006 Nov; 18(5):799-806. PubMed ID: 17016608
    [TBL] [Abstract][Full Text] [Related]  

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

  • 10. 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; 10(6):351-61. PubMed ID: 12080386
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome.
    Durkin ME; Keck-Waggoner CL; Popescu NC; Thorgeirsson SS
    Genomics; 2001 Apr; 73(1):20-7. PubMed ID: 11352562
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 36(2):328-36. PubMed ID: 8812460
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 7(7):737-47. PubMed ID: 10573005
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23.
    Franke Y; Peoples RJ; Francke U
    Cytogenet Cell Genet; 1999; 86(3-4):296-304. PubMed ID: 10575229
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 34(1):17-23. PubMed ID: 8661020
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cloning, expression, and chromosomal mapping of the human 14-3-3gamma gene (YWHAG) to 7q11.23.
    Horie M; Suzuki M; Takahashi E; Tanigami A
    Genomics; 1999 Sep; 60(2):241-3. PubMed ID: 10486217
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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; 113(2):46-9. PubMed ID: 10425618
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A mouse single-copy gene, Gtf2i, the homolog of human GTF2I, that is duplicated in the Williams-Beuren syndrome deletion region.
    Wang YK; Pérez-Jurado LA; Francke U
    Genomics; 1998 Mar; 48(2):163-70. PubMed ID: 9521869
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes.
    Botta A; Novelli G; Mari A; Novelli A; Sabani M; Korenberg J; Osborne LR; Digilio MC; Giannotti A; Dallapiccola B
    J Med Genet; 1999 Jun; 36(6):478-80. PubMed ID: 10874638
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Williams-Beuren Syndrome and Burkitt Leukemia.
    Zhukova N; Naqvi A
    J Pediatr Hematol Oncol; 2013 Jan; 35(1):e30-2. PubMed ID: 23018576
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.