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Journal Abstract Search

202 related items for PubMed ID: 1356379

  • 21. Identification of the I507 deletion by site-directed mutagenesis.
    Orozco L, Friedman K, Chávez M, Lezana JL, Villarreal MT, Carnevale A.
    Am J Med Genet; 1994 Jun 01; 51(2):137-9. PubMed ID: 8092189
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  • 22. Preliminary results on cystic fibrosis haplotypes from patients diagnosed in Odessa.
    De Benedetti L, Ronchetto P, Devoto M, Romeo G, Krainiaia GV, Reznik BY.
    Acta Univ Carol Med (Praha); 1990 Jun 01; 36(1-4):112-4. PubMed ID: 1983380
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  • 23. Genotyping of the Spanish cystic fibrosis population at the delta F508 mutation site and RFLP linked loci.
    Jaume-Roig B, Simon-Bouy B, Taillandier A, Serre JL, Antich J, Bellon J, Boué J, Boué A.
    Hum Genet; 1990 Sep 01; 85(4):410-1. PubMed ID: 1976593
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  • 24. [Specific gene deletion in patients with cystic fibrosis: pilot study of a small patient cohort].
    Scheurlen W, Jeschke R, Kreth HW.
    Padiatr Grenzgeb; 1991 Sep 01; 30(4):275-81. PubMed ID: 1923546
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  • 25. A long-range restriction map encompassing the cystic fibrosis locus and its closely linked genetic markers.
    Poustka AM, Lehrach H, Williamson R, Bates G.
    Genomics; 1988 May 01; 2(4):337-45. PubMed ID: 2906041
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  • 26. [Molecular genetic analysis of TUB18 and TUB20 intragenic polymorphism and various mutations of the CFTR gene in the Moscow region].
    Sazonova MA, Amosenko FA, Kapranov NI, Kalinin VN.
    Genetika; 1997 Sep 01; 33(9):1303-7. PubMed ID: 9445824
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  • 27. [Allele polymorphism of the DNA loci MET, D7S8, D7S23, linked to the cystic fibrosis gene in some populations of the USSR, in high risk families and in cystic fibrosis patients].
    Baranov VS, Ivashchenko TE, Gorbunova VN, Voronina OV, Gaĭtskhoki VS, Gol'tsov AA, Kaboev OK, Shvarts EI, Berlin IuA, Livshits LA.
    Genetika; 1991 Jan 01; 27(1):113-21. PubMed ID: 2037248
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  • 30. The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and Arabs.
    Lerer I, Cohen S, Chemke M, Sanilevich A, Rivlin J, Golan A, Yahav J, Friedman A, Abeliovich D.
    Hum Genet; 1990 Sep 01; 85(4):416-7. PubMed ID: 1976595
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  • 33. Molecular genetic studies in monogenic and polygenic human diseases.
    Endreffy E, László, Szabó A, Román F, Kürti K, Kálmán M, Raskó I.
    Acta Biol Hung; 1997 Sep 01; 48(1):121-8. PubMed ID: 9199707
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  • 34. [Frequency of delta F508 mutation in Venezuelan patients with cystic fibrosis].
    Morales-Machin A, Borjas-Fajardo L, Pineda L, González S, Delgado W, Zabala W, Fernández E.
    Invest Clin; 2004 Jun 01; 45(2):121-30. PubMed ID: 15211979
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  • 35. Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population.
    Vidaud M, Kitzis A, Ferec C, Bozon D, Dumur V, Giraud G, David F, Pascal O, Auvinet M, Morel Y.
    Hum Genet; 1989 Jan 01; 81(2):183-4. PubMed ID: 2563252
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  • 40. Analysis of DNA probes for the prenatal diagnosis of cystic fibrosis.
    Dry PJ, Wake S, Robertson CF, Colley P, Sheffield LJ.
    Med J Aust; 1989 Aug 07; 151(3):131, 133-6. PubMed ID: 2569157
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