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Journal Abstract Search

100 related items for PubMed ID: 3268039

  • 1.
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  • 3. Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markers.
    Middleton-Price HR, Harding AE, Berciano J, Pastor JM, Huson SM, Malcolm S.
    Genomics; 1989 Feb; 4(2):192-7. PubMed ID: 2737679
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  • 4. The hypervariable gene locus PUM, which codes for the tumour associated epithelial mucins, is located on chromosome 1, within the region 1q21-24.
    Swallow DM, Gendler S, Griffiths B, Kearney A, Povey S, Sheer D, Palmer RW, Taylor-Papadimitriou J.
    Ann Hum Genet; 1987 Oct; 51(4):289-94. PubMed ID: 3447512
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  • 5. Regional chromosomal localisation of APOA2 to 1q21-1q23.
    Middleton-Price HR, van den Berghe JA, Scott J, Knott TJ, Malcolm S.
    Hum Genet; 1988 Jul; 79(3):283-5. PubMed ID: 3136074
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  • 6. Linkage analysis of Charcot-Marie-Tooth neuropathy (HMSN type I).
    Ionasescu V, Murray JC, Burns TL, Ionasescu R, Ferrell R, Searby C, Chirgwin J.
    J Neurol Sci; 1987 Aug; 80(1):73-8. PubMed ID: 3302118
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  • 8. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
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  • 9. Localization and linkage of three polymorphic DNA sequences on human chromosome 20.
    Goodfellow PJ, Duncan AM, Farrer LA, Holden JJ, White BN, Kidd JR, Kidd KK, Simpson NE.
    Cytogenet Cell Genet; 1987 Jan; 44(2-3):112-7. PubMed ID: 2882953
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  • 10. Very close linkage between D2S1 and ACP1 on chromosome 2p.
    Lothe RA, Gedde-Dahl T, Olaisen B, Bakker E, Pearson P.
    Ann Hum Genet; 1986 Oct; 50(4):361-7. PubMed ID: 3481680
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  • 14. Establishment of a molecular genetic map of distal mouse chromosome 1: further definition of a conserved linkage group syntenic with human chromosome 1q.
    Seldin MF, Morse HC, LeBoeuf RC, Steinberg AD.
    Genomics; 1988 Jan; 2(1):48-56. PubMed ID: 3384439
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  • 15. Isolation and use of chromosome 1 probes for linkage studies on Charcot-Marie-Tooth disease.
    Griffiths LR, Zwi MB, Mesterovic N, Ross DA, Board PG, Callen DF, Mohandas T, Buckland R, Fletcher JM, Driesel AJ.
    Ann Hum Genet; 1990 Jan; 54(1):31-7. PubMed ID: 2321912
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  • 17. A genetic polymorphism of a human urinary mucin.
    Karlsson S, Swallow DM, Griffiths B, Corney G, Hopkinson DA, Dawnay A, Cartron JP.
    Ann Hum Genet; 1983 Oct; 47(4):263-9. PubMed ID: 6651217
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  • 18. Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpoint.
    Walder RY, Shalev H, Brennan TM, Carmi R, Elbedour K, Scott DA, Hanauer A, Mark AL, Patil S, Stone EM, Sheffield VC.
    Hum Mol Genet; 1997 Sep; 6(9):1491-7. PubMed ID: 9285786
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  • 19. The human tumour-associated epithelial mucins are coded by an expressed hypervariable gene locus PUM.
    Swallow DM, Gendler S, Griffiths B, Corney G, Taylor-Papadimitriou J, Bramwell ME.
    Nature; 1997 Sep; 328(6125):82-4. PubMed ID: 3600778
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  • 20. Localization of the gene encoding human factor V to chromosome 1q21-25.
    Wang H, Riddell DC, Guinto ER, MacGillivray RT, Hamerton JL.
    Genomics; 1988 May; 2(4):324-8. PubMed ID: 3220473
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