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Journal Abstract Search

178 related items for PubMed ID: 3115094

  • 21. Saturation of human chromosome 3 with unique sequence hybridization probes.
    Smith DI, Mangrulker R, Geist R, Gilbert J, Kinsman K, Drabkin H, Golembieski W.
    Genomics; 1989 May; 4(4):453-9. PubMed ID: 2744758
    [Abstract] [Full Text] [Related]

  • 22. Regional localization of the gene for thyroid peroxidase to human chromosome 2pter----p12.
    de Vijlder JJ, Dinsart C, Libert F, Geurts van Kessel A, Bikker H, Bolhuis PA, Vassart G.
    Cytogenet Cell Genet; 1988 May; 47(3):170-2. PubMed ID: 3378456
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  • 23. The Mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease.
    Hill ME, Davies KE, Harper P, Williamson R.
    Hum Genet; 1982 May; 60(3):222-6. PubMed ID: 6286461
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  • 24. Assignment of the human moesin gene (MSN) to chromosome region Xq11.2-->q12.
    Kishino T, Ariga T, Soejima H, Tamura T, Ohta T, Jinno Y, Yonemura S, Sato N, Tsukita S, Tsukita S.
    Cytogenet Cell Genet; 1994 May; 66(3):167-9. PubMed ID: 8125014
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  • 25. Assignment of the gene for the beta subunit of thyroid-stimulating hormone to the short arm of human chromosome 1.
    Dracopoli NC, Rettig WJ, Whitfield GK, Darlington GJ, Spengler BA, Biedler JL, Old LJ, Kourides IA.
    Proc Natl Acad Sci U S A; 1986 Mar; 83(6):1822-6. PubMed ID: 3006075
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  • 26. Detection of the thyroxine-binding globulin (TBG) gene in six unrelated families with complete TBG deficiency.
    Mori Y, Refetoff S, Flink IL, Charbonneau M, Murata Y, Seo H, Morkin E, Dussault JH.
    J Clin Endocrinol Metab; 1988 Oct; 67(4):727-33. PubMed ID: 2901429
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  • 28. A cytochrome P-450 gene family mapped to human chromosome 19.
    Phillips IR, Shephard EA, Povey S, Davis MB, Kelsey G, Monteiro M, West LF, Cowell J.
    Ann Hum Genet; 1985 Oct; 49(4):267-74. PubMed ID: 3000277
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  • 29. Assignment of the human tyrosine aminotransferase gene to chromosome 16.
    Natt E, Kao FT, Rettenmeier R, Scherer G.
    Hum Genet; 1986 Mar; 72(3):225-8. PubMed ID: 2870018
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  • 33. Isolation and characterization of a major tandem repeat family from the human X chromosome.
    Willard HF, Smith KD, Sutherland J.
    Nucleic Acids Res; 1983 Apr 11; 11(7):2017-33. PubMed ID: 6300789
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  • 34. Fine structure physical mapping of the region of mouse chromosome 10 homologous to human chromosome 21.
    MacDonald G, Chu ML, Cox DR.
    Genomics; 1991 Oct 11; 11(2):317-23. PubMed ID: 1837533
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  • 35. cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31.
    Mattei MG, Weil D, Pribula-Conway D, Bernard MP, Passage E, Van Cong N, Timpl R, Chu ML.
    Hum Genet; 1988 Jul 11; 79(3):235-41. PubMed ID: 3402995
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  • 39. Transformation associated p53 protein is encoded by a gene on human chromosome 17.
    Benchimol S, Lamb P, Crawford LV, Sheer D, Shows TB, Bruns GA, Peacock J.
    Somat Cell Mol Genet; 1985 Sep 11; 11(5):505-10. PubMed ID: 2994241
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