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PUBMED FOR HANDHELDS

Journal Abstract Search


53 related items for PubMed ID: 8825609

  • 21. [Evaluation of the association between microsatellite markers located on 6p22-25 and no syndromic cleft lip palate using the case-parents trio design in Chilean population ].
    Blanco R, Suazo J, Santos JL, Carreño H, Paredes M, Jara L, Eltit F.
    Rev Med Chil; 2003 Jul; 131(7):765-72. PubMed ID: 14513697
    [Abstract] [Full Text] [Related]

  • 22. Radiation hybrid and linkage mapping of six new type I markers in the horse.
    Bricker SJ, Brault LS, DelValle A, Millon LV, Murray JD, Penedo MC.
    Anim Genet; 2005 Apr; 36(2):182-4. PubMed ID: 15771743
    [No Abstract] [Full Text] [Related]

  • 23. Ordering of 44 genetic markers in the 6p22 cytogenetic band.
    Trettel F, Malaspina P, Blasi P, Jodice C, Novelletto A, Sabbadini G, Veneziano L, Frontali M, Terrenato L.
    DNA Seq; 1996 Apr; 7(1):51-2. PubMed ID: 9063639
    [No Abstract] [Full Text] [Related]

  • 24. A detailed physical map of the 6p reading disability locus, including new markers and confirmation of recombination suppression.
    Ahn J, Won TW, Kaplan DE, Londin ER, Kuzmic P, Gelernter J, Gruen JR.
    Hum Genet; 2002 Oct; 111(4-5):339-49. PubMed ID: 12384775
    [Abstract] [Full Text] [Related]

  • 25. Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues.
    Pasteris NG, Gorski JL.
    Genomics; 1999 Aug 15; 60(1):57-66. PubMed ID: 10458911
    [Abstract] [Full Text] [Related]

  • 26. Physical and transcript map of the region between D6S264 and D6S149 on chromosome 6q27, the minimal region of allele loss in sporadic epithelial ovarian cancer.
    Liu Y, Emilion G, Mungall AJ, Dunham I, Beck S, Le Meuth-Metzinger VG, Shelling AN, Charnock FM, Ganesan TS.
    Oncogene; 2002 Jan 17; 21(3):387-99. PubMed ID: 11821951
    [Abstract] [Full Text] [Related]

  • 27. Genomic structure of a 200kb region between HLA-C and TNF: implications for transplantation, autoimmune disease and evolution.
    Townend DC, Gaudieri S, Leelayuwat C, Tay GK, Degli-Esposti MP, Dawkins RL.
    DNA Seq; 1996 Jan 17; 7(1):55-9. PubMed ID: 9063641
    [No Abstract] [Full Text] [Related]

  • 28. Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.
    Innis JW, Asher JH, Liang Y, Wang A, Wilke CM, Dierick HA, Kazen-Gillespie K, Sheldon S, Glover TW, Friedman TB.
    Am J Med Genet; 1997 Aug 22; 71(3):292-7. PubMed ID: 9268099
    [Abstract] [Full Text] [Related]

  • 29. Mapping of human interferon regulatory factor 3 (IRF3) to chromosome 19q13.3-13.4 by an intragenic polymorphic marker.
    Bellingham J, Gregory-Evans K, Gregory-Evans CY.
    Ann Hum Genet; 1998 May 22; 62(Pt 3):231-4. PubMed ID: 9803267
    [Abstract] [Full Text] [Related]

  • 30. Precise localization of D11S1226 to the human EMK1 gene at chromosome band 11q13 by sequence homology search.
    Navarro E.
    Cytogenet Cell Genet; 1999 May 22; 86(1):66-7. PubMed ID: 10516437
    [No Abstract] [Full Text] [Related]

  • 31. Assignment of the human metabotropic glutamate receptor gene GRM4 to chromosome 6 band p21.3 by radiation hybrid mapping.
    Barbon A, Ferraboli S, Barlati S.
    Cytogenet Cell Genet; 2000 May 22; 88(3-4):210. PubMed ID: 10828590
    [No Abstract] [Full Text] [Related]

  • 32. A cosmid clone at the D6S182 locus on human chromosome 6p12 contains the 90-kDa heat shock protein beta gene (HSP90 beta).
    Takahashi I, Tanuma R, Hirata M, Hashimoto K.
    Mamm Genome; 1994 Feb 22; 5(2):121-2. PubMed ID: 8180474
    [No Abstract] [Full Text] [Related]

  • 33. Assignment of liver-specific organic anion transporter (SLC22A7) to human chromosome 6 bands p21.2-->p21.1 using radiation hybrids.
    Kok LD, Siu SS, Fung KP, Tsui SK, Lee CY, Waye MM.
    Cytogenet Cell Genet; 2000 Feb 22; 88(1-2):76-7. PubMed ID: 10773670
    [No Abstract] [Full Text] [Related]

  • 34. [Malignant hyperthermia is genetically heterogenetic. Problems in search for molecular genetic markers].
    Deufel T.
    Fortschr Med; 1992 Jan 20; 110(1-2):49. PubMed ID: 1563699
    [No Abstract] [Full Text] [Related]

  • 35. An integrated genetic map of Chromosome 6.
    Cooke IE, Cox SA, Shelling AN, Le Meuth VG, Spurr NK, Ganesan TS.
    Mamm Genome; 1996 Feb 20; 7(2):157-9. PubMed ID: 8835537
    [No Abstract] [Full Text] [Related]

  • 36. The Chromosome 6 database at the Sanger Centre.
    Theaker AJ, Maslen GL, Scott CE, Rice CM, Hunt SE, King A, Mungall AJ, Dunham I, Beck S.
    DNA Seq; 1997 Feb 20; 8(3):167-71. PubMed ID: 10668963
    [Abstract] [Full Text] [Related]

  • 37. Proceedings of the 1st Chromosome 6 Sequencing Meeting. Hinxton, England, March 20, 1996.
    DNA Seq; 1996 Feb 20; 7(1):1-62. PubMed ID: 9147619
    [No Abstract] [Full Text] [Related]

  • 38. Report of the committee on the genetic constitution of chromosome 6.
    Ziegler A, Field LL, Sakaguchi AY.
    Cytogenet Cell Genet; 1990 Feb 20; 55(1-4):118-21. PubMed ID: 2073824
    [No Abstract] [Full Text] [Related]

  • 39. Report of the committee on the genetic constitution of chromosome 6.
    Spence MA, Spurr NK, Field LL.
    Cytogenet Cell Genet; 1989 Feb 20; 51(1-4):149-65. PubMed ID: 2676368
    [No Abstract] [Full Text] [Related]

  • 40. Short report on DNA marker at candidate locus.
    Patsalis PC, Ozer HL, Henderson AS.
    Clin Genet; 1995 Nov 20; 48(5):275-6. PubMed ID: 8825609
    [No Abstract] [Full Text] [Related]


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