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Journal Abstract Search

170 related items for PubMed ID: 9503011

  • 1. Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome.
    Dahmane N, Ghezala GA, Gosset P, Chamoun Z, Dufresne-Zacharia MC, Lopes C, Rabatel N, Gassanova-Maugenre S, Chettouh Z, Abramowski V, Fayet E, Yaspo ML, Korn B, Blouin JL, Lehrach H, Poutska A, Antonarakis SE, Sinet PM, Créau N, Delabar JM.
    Genomics; 1998 Feb 15; 48(1):12-23. PubMed ID: 9503011
    [Abstract] [Full Text] [Related]

  • 2. Cosmid contig and transcriptional map of three regions of human chromosome 21q22: identification of 37 novel transcripts by direct selection.
    Guimera J, Pucharcós C, Domènech A, Casas C, Solans A, Gallardo T, Ashley J, Lovett M, Estivill X, Pritchard M.
    Genomics; 1997 Oct 01; 45(1):59-67. PubMed ID: 9339361
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  • 3. An integrated map with cosmid/PAC contigs of a 4-Mb Down syndrome critical region.
    Osoegawa K, Susukida R, Okano S, Kudoh J, Minoshima S, Shimizu N, de Jong PJ, Groet J, Ives J, Lehrach H, Nizetic D, Soeda E.
    Genomics; 1996 Mar 15; 32(3):375-87. PubMed ID: 8838801
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  • 4. 3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21.
    Dufresne-Zacharia MC, Dahmane N, Theophile D, Orti R, Chettouh Z, Sinet PM, Delabar JM.
    Genomics; 1994 Feb 15; 19(3):462-9. PubMed ID: 8188288
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  • 5. High resolution physical mapping and identification of transcribed sequences in the Down syndrome region-2.
    Vidal-Taboada JM, Bergoñón S, Sánchez M, López-Acedo C, Groet J, Nizetic D, Egeo A, Scartezzini P, Katsanis N, Fisher EM, Delabar JM, Oliva R.
    Biochem Biophys Res Commun; 1998 Feb 13; 243(2):572-8. PubMed ID: 9480850
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  • 10. Cloning of a novel homeobox-containing gene, PKNOX1, and mapping to human chromosome 21q22.3.
    Chen H, Rossier C, Nakamura Y, Lynn A, Chakravarti A, Antonarakis SE.
    Genomics; 1997 Apr 15; 41(2):193-200. PubMed ID: 9143494
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  • 12. Isolation of genes from the Batten candidate region using exon amplification. Batten Disease Consortium.
    Lerner TJ, D'Arigo KL, Haines JL, Doggett NA, Taschner PE, de Vos N, Buckler AJ.
    Am J Med Genet; 1995 Jun 05; 57(2):320-3. PubMed ID: 7668355
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  • 14. A contiguous 3-Mb sequence-ready map in the S3-MX region on 21q22.2 based on high- throughput nonisotopic library screenings.
    Hildmann T, Kong X, O'Brien J, Riesselman L, Christensen HM, Dagand E, Lehrach H, Yaspo ML.
    Genome Res; 1999 Apr 05; 9(4):360-72. PubMed ID: 10207158
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  • 15. A transcript map of the Down syndrome critical region on chromosome 21.
    Peterson A, Patil N, Robbins C, Wang L, Cox DR, Myers RM.
    Hum Mol Genet; 1994 Oct 05; 3(10):1735-42. PubMed ID: 7849696
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  • 16. Transcription mapping in a medulloblastoma breakpoint interval and Smith-Magenis syndrome candidate region: identification of 53 transcriptional units and new candidate genes.
    Seranski P, Heiss NS, Dhorne-Pollet S, Radelof U, Korn B, Hennig S, Backes E, Schmidt S, Wiemann S, Schwarz CE, Lehrach H, Poustka A.
    Genomics; 1999 Feb 15; 56(1):1-11. PubMed ID: 10036180
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  • 17. A search for genes from the dark band regions of human chromosome 21.
    Xu H, Wei H, Tassone F, Graw S, Gardiner K, Weissman SM.
    Genomics; 1995 May 01; 27(1):1-8. PubMed ID: 7665155
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  • 18. Physical and transcription map in the region 14q24.3: identification of six novel transcripts.
    Roux AF, Rommens JM, Read L, Duncan AM, Cox DW.
    Genomics; 1997 Jul 15; 43(2):130-40. PubMed ID: 9244429
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  • 19. Isolation and mapping of human chromosome 21 cDNA: progress in constructing a chromosome 21 expression map.
    Cheng JF, Boyartchuk V, Zhu Y.
    Genomics; 1994 Sep 01; 23(1):75-84. PubMed ID: 7829105
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  • 20. A 1.6-Mb P1-based physical map of the Down syndrome region on chromosome 21.
    Ohira M, Ichikawa H, Suzuki E, Iwaki M, Suzuki K, Saito-Ohara F, Ikeuchi T, Chumakov I, Tanahashi H, Tashiro K, Sakaki Y.
    Genomics; 1996 Apr 01; 33(1):65-74. PubMed ID: 8617511
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