These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


188 related items for PubMed ID: 8088786

  • 21. Physical linkage of the human growth hormone gene cluster and the skeletal muscle sodium channel alpha-subunit gene (SCN4A) on chromosome 17.
    Bennani-Baiti IM, Jones BK, Liebhaber SA, Cooke NE.
    Genomics; 1995 Oct 10; 29(3):647-52. PubMed ID: 8575757
    [Abstract] [Full Text] [Related]

  • 22. YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.
    Wedemeyer N, Lengeling A, Ronsiek M, Korthaus D, Baer K, Wuttke M, Jockusch H.
    Genomics; 1996 Mar 15; 32(3):447-54. PubMed ID: 8838809
    [Abstract] [Full Text] [Related]

  • 23. Refined mapping of the human Ets-related gene Elk-1 to Xp11.2-p11.4, distal to the OATL1 region.
    Janz M, Lehmann U, Olde Weghuis D, de Leeuw B, Geurts van Kessel A, Gilgenkrantz S, Hipskind RA, Nordheim A.
    Hum Genet; 1994 Oct 15; 94(4):442-4. PubMed ID: 7927346
    [Abstract] [Full Text] [Related]

  • 24. Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41.
    Rosati M, Franzé A, Matarazzo MR, Grimaldi G.
    Cytogenet Cell Genet; 1999 Oct 15; 85(3-4):291-6. PubMed ID: 10449920
    [Abstract] [Full Text] [Related]

  • 25. GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families.
    Vortkamp A, Gessler M, Grzeschik KH.
    Nature; 1991 Aug 08; 352(6335):539-40. PubMed ID: 1650914
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Cloning and characterization of ZNF189, a novel human Krüppel-like zinc finger gene localized to chromosome 9q22-q31.
    Odeberg J, Røsok O, Gudmundsson GH, Ahmadian A, Roshani L, Williams C, Larsson C, Pontén F, Uhlén M, Asheim HC, Lundeberg J.
    Genomics; 1998 Jun 01; 50(2):213-21. PubMed ID: 9653648
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Physical linkage of the murine Hox-b cluster and nerve growth factor receptor on yeast artificial chromosomes.
    Bentley KL, Bradshaw MS, Ruddle FH.
    Genomics; 1993 Oct 01; 18(1):43-53. PubMed ID: 7903957
    [Abstract] [Full Text] [Related]

  • 32. A 9.75-Mb map across the centromere of human chromosome 10.
    Jackson MS, See CG, Mulligan LM, Lauffart BF.
    Genomics; 1996 Apr 15; 33(2):258-70. PubMed ID: 8660974
    [Abstract] [Full Text] [Related]

  • 33. 2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes.
    Lafrenière RG, Brown CJ, Rider S, Chelly J, Taillon-Miller P, Chinault AC, Monaco AP, Willard HF.
    Hum Mol Genet; 1993 Aug 15; 2(8):1105-15. PubMed ID: 8401491
    [Abstract] [Full Text] [Related]

  • 34. A YAC contig spanning a cluster of human type III receptor protein tyrosine kinase genes (PDGFRA-KIT-KDR) in chromosome segment 4q12.
    Spritz RA, Strunk KM, Lee ST, Lu-Kuo JM, Ward DC, Le Paslier D, Altherr MR, Dorman TE, Moir DT.
    Genomics; 1994 Jul 15; 22(2):431-6. PubMed ID: 7528718
    [Abstract] [Full Text] [Related]

  • 35. Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig.
    Gorski JL, Bialecki MD, McDonald MT, Massa HF, Trask BJ, Burright EN.
    Genomics; 1996 Jul 15; 35(2):338-45. PubMed ID: 8661147
    [Abstract] [Full Text] [Related]

  • 36. [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 15; 24(2):99-108. PubMed ID: 9254964
    [Abstract] [Full Text] [Related]

  • 37. Characterization of the C3 YAC contig from proximal mouse chromosome 17 and analysis of allelic expression of genes flanking the imprinted Igf2r gene.
    Schweifer N, Valk PJ, Delwel R, Cox R, Francis F, Meier-Ewert S, Lehrach H, Barlow DP.
    Genomics; 1997 Aug 01; 43(3):285-97. PubMed ID: 9268631
    [Abstract] [Full Text] [Related]

  • 38. Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich interval.
    Schindelhauer D, Hellebrand H, Grimm L, Bader I, Meitinger T, Wehnert M, Ross M, Meindl A.
    Genome Res; 1996 Nov 01; 6(11):1056-69. PubMed ID: 8938429
    [Abstract] [Full Text] [Related]

  • 39. Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene.
    Biancalana V, Trivier E, Weber C, Weissenbach J, Rowe PS, O'Riordan JL, Partington MW, Heyberger S, Oudet C, Hanauer A.
    Genomics; 1994 Aug 01; 22(3):617-25. PubMed ID: 8001973
    [Abstract] [Full Text] [Related]

  • 40. A YAC contig of the human CC chemokine genes clustered on chromosome 17q11.2.
    Naruse K, Ueno M, Satoh T, Nomiyama H, Tei H, Takeda M, Ledbetter DH, Coillie EV, Opdenakker G, Gunge N, Sakaki Y, Iio M, Miura R.
    Genomics; 1996 Jun 01; 34(2):236-40. PubMed ID: 8661057
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 10.