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Journal Abstract Search

198 related items for PubMed ID: 3019869

  • 21. Isolation of a polymorphic DNA segment unique to human chromosome 7 by molecular cloning of hybrid cell DNA.
    Humphries P, Barton D, McKay AM, Humphries MM, Carritt B.
    Mol Gen Genet; 1983; 190(1):143-9. PubMed ID: 6304471
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  • 22. Molecular characterization of the purity of seven human chromosome-specific DNA libraries.
    Perlman J, Fuscoe JC.
    Cytogenet Cell Genet; 1986; 43(1-2):87-96. PubMed ID: 3780320
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  • 23. High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q.
    Bengtsson U, Altherr MR, Wasmuth JJ, Winokur ST.
    Hum Mol Genet; 1994 Oct; 3(10):1801-5. PubMed ID: 7849703
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  • 25. Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.
    de Martinville B, Kunkel LM, Bruns G, Morlé F, Koenig M, Mandel JL, Horwich A, Latt SA, Gusella JF, Housman D.
    Am J Hum Genet; 1985 Mar; 37(2):235-49. PubMed ID: 2984924
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  • 27. Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals.
    Petit C, Levilliers J, Rouyer F, Simmler MC, Herouin E, Weissenbach J.
    Genomics; 1990 Apr; 6(4):651-8. PubMed ID: 2341154
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  • 29. Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.
    Mattei MG, Baeteman MA, Heilig R, Oberlé I, Davies K, Mandel JL, Mattei JF.
    Hum Genet; 1985 Apr; 69(4):327-31. PubMed ID: 2985491
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  • 30. The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22----q24) by somatic cell hybrid analysis and in situ hybridization.
    Barton DE, Yang-Feng TL, Francke U.
    Hum Genet; 1986 Mar; 72(3):221-4. PubMed ID: 2870017
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  • 33. Organization and chromosomal specificity of autosomal homologs of human Y chromosome repeated DNA.
    Burk RD, Szabo P, O'Brien S, Nash WG, Yu L, Smith KD.
    Chromosoma; 1985 Mar; 92(3):225-33. PubMed ID: 2990828
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  • 34. Assignment of the human gamma-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33-36.
    Shiloh Y, Donlon T, Bruns G, Breitman ML, Tsui LC.
    Hum Genet; 1986 May; 73(1):17-9. PubMed ID: 3011643
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  • 37. Human chromosome-specific DNA libraries: construction and purity analysis.
    Fuscoe JC, McNinch JS, Collins CC, Van Dilla MA.
    Cytogenet Cell Genet; 1989 May; 50(4):211-5. PubMed ID: 2680305
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