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Journal Abstract Search

153 related items for PubMed ID: 1713272

  • 1. Genetic analysis in cystic fibrosis using the amplification refractory mutation system (ARMS): the J3.11 MspI polymorphism.
    Newton CR, Summers C, Heptinstall LE, Lynch JR, Finniear RS, Ogilvie D, Smith JC, Markham AF.
    J Med Genet; 1991 Apr; 28(4):248-51. PubMed ID: 1713272
    [Abstract] [Full Text] [Related]

  • 2. Polymerase chain reaction for detection of the pMP6d-9/MspI RFLP, a marker closely linked to the cystic fibrosis mutation.
    Huth A, Estivill X, Grade K, Billwitz H, Speer A, Rosenthal A, Williamson R, Ramsay M, Coutelle C.
    Nucleic Acids Res; 1989 Sep 12; 17(17):7118. PubMed ID: 2476727
    [No Abstract] [Full Text] [Related]

  • 3. Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locus.
    Stanier P, Estivill X, Lench N, Williamson R.
    Hum Genet; 1988 Nov 12; 80(3):309-10. PubMed ID: 2461342
    [Abstract] [Full Text] [Related]

  • 4. MspI restriction fragment length polymorphism near exon 10 of cystic fibrosis (CFTR) gene.
    Bosch A, Kruyer H, Nunes V, Estivill X.
    Nucleic Acids Res; 1991 Apr 11; 19(7):1719. PubMed ID: 1709281
    [No Abstract] [Full Text] [Related]

  • 5. Amplification refractory mutation system for prenatal diagnosis and carrier assessment in cystic fibrosis.
    Newton CR, Heptinstall LE, Summers C, Super M, Schwarz M, Anwar R, Graham A, Smith JC, Markham AF.
    Lancet; 1991 Apr 11; 2(8678-8679):1481-3. PubMed ID: 2574768
    [Abstract] [Full Text] [Related]

  • 6. A cystic fibrosis patient with delta F508, G542X and a deletion at the D7S8 locus.
    Wagner K, Greil I, Schneditz P, Pommer M, Rosenkranz W.
    Hum Mutat; 1994 Apr 11; 3(3):327-9. PubMed ID: 7517267
    [No Abstract] [Full Text] [Related]

  • 7. Detection of a rare allele with the pMP6d-9/MspI RFLP near the cystic fibrosis locus.
    Nunes V, Casals T, Gallano P, Giménez FJ, Kere J, Williamson R, Estivill X.
    Hum Genet; 1989 Oct 11; 83(3):305-6. PubMed ID: 2571567
    [Abstract] [Full Text] [Related]

  • 8. Rapid communication: MspI restriction fragment length polymorphism at the swine myogenin locus.
    Ernst CW, Vaske DA, Larson RG, Rothschild MF.
    J Anim Sci; 1993 Dec 11; 71(12):3479. PubMed ID: 7507477
    [No Abstract] [Full Text] [Related]

  • 9. MspI RFLP at 19q13.3 identified by the anonymous DNA sequence pX75B (D19S112).
    Hermens R, Coerwinkel M, Brunner H, Smeets H, Wieringa B.
    Nucleic Acids Res; 1991 Apr 11; 19(7):1726. PubMed ID: 1709283
    [No Abstract] [Full Text] [Related]

  • 10. An MspI polymorphism at the D7S599E locus.
    Hampson RM, Black GC, Leung LS, Jones SE, Neal MJ.
    Hum Mol Genet; 1993 Sep 11; 2(9):1510. PubMed ID: 7694729
    [No Abstract] [Full Text] [Related]

  • 11. MspI RFLP in the gene for a type I intermediate filament wool keratin.
    Rogers GR, Hickford JG, Bickerstaffe R.
    Anim Genet; 1993 Jun 11; 24(3):218. PubMed ID: 7689799
    [No Abstract] [Full Text] [Related]

  • 12. An MspI polymorphism in the hyman serotonin receptor gene (HTR2): detection by DGGE and RFLP analysis.
    Warren JT, Peacock ML, Rodriguez LC, Fink JK.
    Hum Mol Genet; 1993 Mar 11; 2(3):338. PubMed ID: 7684645
    [No Abstract] [Full Text] [Related]

  • 13. Additional polymorphism for D7S8 linked to cystic fibrosis including detection by DNA amplification.
    Northrup H, Rosenbloom C, O'Brien WE, Beaudet AL.
    Nucleic Acids Res; 1989 Feb 25; 17(4):1784. PubMed ID: 2564190
    [No Abstract] [Full Text] [Related]

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  • 18. A MspI restriction fragment length polymorphism at the ovine locus for glucagon.
    Penty JM, Montgomery GW.
    Anim Genet; 1991 Feb 25; 22(5):440. PubMed ID: 1723255
    [No Abstract] [Full Text] [Related]

  • 19. Two MspI polymorphisms within the APC gene.
    Cottrell S, Bodmer WF.
    Hum Mol Genet; 1992 Aug 25; 1(5):352. PubMed ID: 1284630
    [No Abstract] [Full Text] [Related]

  • 20. PCR detection of the MspI polymorphism in the human IRBP gene (RPB3).
    Wu J, Nickerson JM.
    Nucleic Acids Res; 1991 Jul 25; 19(14):4016. PubMed ID: 1713667
    [No Abstract] [Full Text] [Related]

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