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Journal Abstract Search

145 related items for PubMed ID: 8353486

  • 1.
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  • 2. Refinement of linkage of human severe combined immunodeficiency (SCIDX1) to polymorphic markers in Xq13.
    Puck JM, Conley ME, Bailey LC.
    Am J Hum Genet; 1993 Jul; 53(1):176-84. PubMed ID: 8317482
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  • 3. The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.
    Puck JM, Deschênes SM, Porter JC, Dutra AS, Brown CJ, Willard HF, Henthorn PS.
    Hum Mol Genet; 1993 Aug; 2(8):1099-104. PubMed ID: 8401490
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  • 4. Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome.
    Lindsay S, Curtis AR, Roustan P, Kamakari S, Thiselton DL, Stephenson A, Bhattacharya SS.
    Genomics; 1993 Jul; 17(1):208-10. PubMed ID: 8406451
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  • 5. Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3.
    Wirth B, Pick E, Leutner A, Dadze A, Voosen B, Knapp M, Piechaczek-Wappenschmidt B, Rudnik-Schöneborn S, Schönling J, Cox S.
    Genomics; 1994 Mar 01; 20(1):84-93. PubMed ID: 7912691
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  • 6. Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21.
    Clark PA, Lester T, Villard L, Fontes M, Kinnon C.
    J Med Genet; 1994 Apr 01; 31(4):344-5. PubMed ID: 8071966
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  • 7. MAF45, a highly polymorphic marker for the pseudoautosomal region of the sheep genome, is not linked to the FecXI (Inverdale) gene.
    Swarbrick PA, Schmack AE, Crawford AM.
    Genomics; 1992 Jul 01; 13(3):849-51. PubMed ID: 1639413
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  • 9. A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus.
    White A, Tomfohrde J, Stewart E, Barnes R, Le Paslier D, Weissenbach J, Cavalli-Sforza L, Farrer L, Bowcock A.
    Proc Natl Acad Sci U S A; 1993 Nov 01; 90(21):10105-9. PubMed ID: 8234264
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  • 10. Mapping of the pulmonary surfactant SP5 (SFTP2) locus to 8p21 and characterization of a microsatellite repeat marker that shows frequent loss of heterozygosity in human carcinomas.
    Wood S, Yaremko ML, Schertzer M, Kelemen PR, Minna J, Westbrook CA.
    Genomics; 1994 Dec 01; 24(3):597-600. PubMed ID: 7713515
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  • 11. Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6.
    Brzustowicz LM, Kleyn PW, Boyce FM, Lien LL, Monaco AP, Penchaszadeh GK, Das K, Wang CH, Munsat TL, Ott J.
    Genomics; 1992 Aug 01; 13(4):991-8. PubMed ID: 1505990
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  • 14. Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA).
    Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Grewal PK, Dennis C, Buckle V, Ignatius J, Dubowitz V.
    Hum Genet; 1993 Sep 01; 92(2):133-8. PubMed ID: 8370578
    [Abstract] [Full Text] [Related]

  • 15. DNA sequence polymorphism at the human tumor necrosis factor (TNF) locus. Numerous TNF/lymphotoxin alleles tagged by two closely linked microsatellites in the upstream region of the lymphotoxin (TNF-beta) gene.
    Nedospasov SA, Udalova IA, Kuprash DV, Turetskaya RL.
    J Immunol; 1991 Aug 01; 147(3):1053-9. PubMed ID: 1861069
    [Abstract] [Full Text] [Related]

  • 16. Physical and genetic mapping in the region of Xq12-21, which contains the locus for X-linked severe combined immunodeficiency.
    Jones A, Morris T, de Alwis M, Malcolm S, Levinsky RJ, Kinnon C.
    Immunodeficiency; 1993 Aug 01; 4(1-4):259-62. PubMed ID: 8167714
    [No Abstract] [Full Text] [Related]

  • 17. Twenty-one polymorphic markers from human chromosome 12 for integration of genetic and physical maps.
    LeBlanc-Straceski JM, Montgomery KT, Kissel H, Murtaugh L, Tsai P, Ward DC, Krauter KS, Kucherlapati R.
    Genomics; 1994 Jan 15; 19(2):341-9. PubMed ID: 8188264
    [Abstract] [Full Text] [Related]

  • 18. Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiency.
    Deschênes SM, Puck JM, Dutra AS, Somberg RL, Felsburg PJ, Henthorn PS.
    Genomics; 1994 Sep 01; 23(1):62-8. PubMed ID: 7829103
    [Abstract] [Full Text] [Related]

  • 19. A microsatellite polymorphism associated with the PLC1 (phospholipase C) locus: identification, mapping, and linkage to the MODY locus on chromosome 20.
    Rothschild CB, Akots G, Fajans SS, Bowden DW.
    Genomics; 1992 Jul 01; 13(3):560-4. PubMed ID: 1639386
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