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PUBMED FOR HANDHELDS

Journal Abstract Search


278 related items for PubMed ID: 8276392

  • 1. A yeast artificial chromosome contig linking the steroid sulfatase and Kallmann syndrome loci on the human X chromosome short arm.
    Lee WC, Ferrero GB, Chinault AC, Yen PH, Ballabio A.
    Genomics; 1993 Oct; 18(1):1-6. PubMed ID: 8276392
    [Abstract] [Full Text] [Related]

  • 2. A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus.
    Lanyi A, Li B, Li S, Talmadge CB, Brichacek B, Davis JR, Kozel BA, Trask B, van den Engh G, Uzvolgyi E, Stanbridge EJ, Nelson DL, Chinault C, Heslop H, Gross TG, Seemayer TA, Klein G, Purtilo DT, Sumegi J.
    Genomics; 1997 Jan 01; 39(1):55-65. PubMed ID: 9027486
    [Abstract] [Full Text] [Related]

  • 3. Isolation and characterization of a yeast artificial chromosome (YAC) contig around the human steroid sulfatase gene.
    Carrozzo R, Ellison J, Yen P, Taillon-Miller P, Brownstein BH, Persico G, Ballabio A, Shapiro L.
    Genomics; 1992 Jan 01; 12(1):7-12. PubMed ID: 1733866
    [Abstract] [Full Text] [Related]

  • 4. Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell lines.
    Francis F, Benham F, See CG, Fox M, Ishikawa-Brush Y, Monaco AP, Weiss B, Rappold G, Hamvas RM, Lehrach H.
    Genomics; 1994 Mar 01; 20(1):75-83. PubMed ID: 8020959
    [Abstract] [Full Text] [Related]

  • 5. A high-density STS map based on a single contig of YAC and P1 clones in the chromosome 8p12-p21 region.
    Mitsuda N, Nakura J, Ye L, Zhao Y, Fujioka Y, Takahashi-Fujii A, Ishino Y, Kato I, Hashimoto K, Ogihara T, Miki T.
    Genomics; 1997 Apr 01; 41(1):49-55. PubMed ID: 9126481
    [Abstract] [Full Text] [Related]

  • 6. [Some YAC contig construction and long range physical mapping at human X chromosome Xp11.3-21.3].
    Miao WM, Wei Y, Deng W, Zhou W, Li HJ, Chal J, Tan J.
    Yi Chuan Xue Bao; 1997 Apr 01; 24(2):99-108. PubMed ID: 9254964
    [Abstract] [Full Text] [Related]

  • 7. Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome.
    Ellison KA, Roth EJ, McCabe ER, Chinault AC, Zoghbi HY.
    Am J Med Genet; 1993 Nov 15; 47(7):1124-34. PubMed ID: 8291533
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  • 9. Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.
    Forbes SA, Brennan L, Richardson M, Coffey A, Cole CG, Gregory SG, Bentley DR, Mumm S, Moore GE, Stanier P.
    Genomics; 1996 Jan 01; 31(1):36-43. PubMed ID: 8808277
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  • 11. A YAC contig of approximately 3 Mb from human chromosome 5q31-->q33.
    Li X, Wise CA, Le Paslier D, Hawkins AL, Griffin CA, Pittler SJ, Lovett M, Jabs EW.
    Genomics; 1994 Feb 01; 19(3):470-7. PubMed ID: 8188289
    [Abstract] [Full Text] [Related]

  • 12. A 2.3-Mb yeast artificial chromosome contig spanning from Gabra3 to G6pd on the mouse X chromosome.
    Chatterjee A, Faust CJ, Molinari-Storey L, Kiochis P, Poustka A, Herman GE.
    Genomics; 1994 May 01; 21(1):49-57. PubMed ID: 8088815
    [Abstract] [Full Text] [Related]

  • 13. A cosmid and yeast artificial chromosome contig containing the complete ryanodine receptor (RYR1) gene.
    Rouquier S, Giorgi D, Trask B, Bergmann A, Phillips MS, MacLennan DH, de Jong P.
    Genomics; 1993 Aug 01; 17(2):330-40. PubMed ID: 8406483
    [Abstract] [Full Text] [Related]

  • 14. An EST and STS-based YAC contig map of human chromosome 9q22.3.
    Lench NJ, Telford EA, Andersen SE, Moynihan TP, Robinson PA, Markham AF.
    Genomics; 1996 Dec 01; 38(2):199-205. PubMed ID: 8954802
    [Abstract] [Full Text] [Related]

  • 15. A YAC contig spanning the hypophosphatemic rickets disease gene (HYP) candidate region.
    Francis F, Rowe PS, Econs MJ, See CG, Benham F, O'Riordan JL, Drezner MK, Hamvas RM, Lehrach H.
    Genomics; 1994 May 01; 21(1):229-37. PubMed ID: 8088792
    [Abstract] [Full Text] [Related]

  • 16. Integrated STS/YAC physical, genetic, and transcript map of human Xq21.3 to q23/q24 (DXS1203-DXS1059).
    Srivastava AK, McMillan S, Jermak C, Shomaker M, Copeland-Yates SA, Sossey-Alaoui K, Mumm S, Schlessinger D, Nagaraja R.
    Genomics; 1999 Jun 01; 58(2):188-201. PubMed ID: 10366451
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  • 18. Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer.
    Hoggard N, Hey Y, Brintnell B, James L, Jones D, Mitchell E, Weissenbach J, Varley JM.
    Genomics; 1995 Nov 20; 30(2):233-43. PubMed ID: 8586422
    [Abstract] [Full Text] [Related]

  • 19. Physical map of mouse chromosome 17 in the region relevant for positional cloning of the Hybrid sterility 1 gene.
    Trachtulec Z, Vincek V, Hamvas RM, Forejt J, Lehrach H, Klein J.
    Genomics; 1994 Sep 01; 23(1):132-7. PubMed ID: 7829061
    [Abstract] [Full Text] [Related]

  • 20. Characterization of the deletion breakpoints in a patient with steroid sulfatase deficiency.
    Yen PH, Ferrero GB, Chinault AC, Mohandas T, Ballabio A.
    Hum Mutat; 1994 Sep 01; 4(1):76-8. PubMed ID: 7951263
    [No Abstract] [Full Text] [Related]


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