These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

92 related items for PubMed ID: 8364537

  • 21. 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; 2(4):337-45. PubMed ID: 2906041
    [Abstract] [Full Text] [Related]

  • 22. [Analysis of the spectra of mutations and polymorphic loci of cystic fibrosis transmembrane conductance regulator in the population of Bashkortostan].
    Korytina GF, Viktorova TV, Baĭkova GV, Khusnutdinova EK.
    Genetika; 2002 Sep; 38(9):1270-5. PubMed ID: 12391889
    [Abstract] [Full Text] [Related]

  • 23. Haplotype analysis of 94 cystic fibrosis mutations with seven polymorphic CFTR DNA markers.
    Morral N, Dörk T, Llevadot R, Dziadek V, Mercier B, Férec C, Costes B, Girodon E, Zielenski J, Tsui LC, Tümmler B, Estivill X.
    Hum Mutat; 1996 Sep; 8(2):149-59. PubMed ID: 8844213
    [Abstract] [Full Text] [Related]

  • 24. Exclusion of human chromosome 13q34 as the site of the cystic fibrosis mutation.
    Scambler PJ, Wainwright BJ, MacGillivray RT, Fung MR, Williamson R.
    Am J Hum Genet; 1986 Apr; 38(4):567-72. PubMed ID: 3010714
    [Abstract] [Full Text] [Related]

  • 25. Joint Bayesian estimation of mutation location and age using linkage disequilibrium.
    Rannala B, Reeve JP.
    Pac Symp Biocomput; 2003 Apr; ():526-34. PubMed ID: 12603055
    [Abstract] [Full Text] [Related]

  • 26. Regional distribution of cystic fibrosis-linked DNA haplotypes in Brazil: multicenter study.
    Raskin S, Philips JA, Krishnamani MR, Vnencak-Jones C, Parker RA, Dawson E, Rozov T, Cardieri JM, Marostica P, Abreu F, Giugliani R, Reis F, Rosario NA, Ludwig N, Culpi L.
    Hum Biol; 1997 Feb; 69(1):75-88. PubMed ID: 9037896
    [Abstract] [Full Text] [Related]

  • 27. Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11.
    Farrall M, Watson E, Bates G, Bell G, Bell J, Davies KA, Estivill X, Kruyer H, Law HY, Lench N.
    Am J Hum Genet; 1986 Dec; 39(6):713-9. PubMed ID: 3467586
    [Abstract] [Full Text] [Related]

  • 28. Allele frequencies of cystic fibrosis-linked markers and F508 deletion in affected Hungarian families.
    Endreffy E, Burg K, Gyurkovits K, Kálmán M, László A, Raskó I.
    Acta Paediatr Hung; 1992 Dec; 32(2):101-13. PubMed ID: 1356379
    [Abstract] [Full Text] [Related]

  • 29. A closely linked genetic marker for cystic fibrosis.
    White R, Woodward S, Leppert M, O'Connell P, Hoff M, Herbst J, Lalouel JM, Dean M, Vande Woude G.
    Nature; 1992 Dec; 318(6044):382-4. PubMed ID: 3906407
    [Abstract] [Full Text] [Related]

  • 30. Comprehensive cystic fibrosis mutation epidemiology and haplotype characterization in a southern Italian population.
    Castaldo G, Polizzi A, Tomaiuolo R, Cazeneuve C, Girodon E, Santostasi T, Salvatore D, Raia V, Rigillo N, Goossens M, Salvatore F.
    Ann Hum Genet; 2005 Jan; 69(Pt 1):15-24. PubMed ID: 15638824
    [Abstract] [Full Text] [Related]

  • 31. Identification of the cystic fibrosis gene: genetic analysis.
    Kerem B, Rommens JM, Buchanan JA, Markiewicz D, Cox TK, Chakravarti A, Buchwald M, Tsui LC.
    Science; 1989 Sep 08; 245(4922):1073-80. PubMed ID: 2570460
    [Abstract] [Full Text] [Related]

  • 32. [Analysis of various polymorphic markers of the CFTR gene in cystic fibrosis patients and healthy donors from the Moscow region].
    Amosenko FA, Sazonova MA, Kapranov NI, Trubnikova IS, Kalinin VN.
    Genetika; 1995 Apr 08; 31(4):532-5. PubMed ID: 7607440
    [Abstract] [Full Text] [Related]

  • 33. ATB(0)/SLC1A5 gene. Fine localisation and exclusion of association with the intestinal phenotype of cystic fibrosis.
    Larriba S, Sumoy L, Ramos MD, Giménez J, Estivill X, Casals T, Nunes V.
    Eur J Hum Genet; 2001 Nov 08; 9(11):860-6. PubMed ID: 11781704
    [Abstract] [Full Text] [Related]

  • 34. [The delta F508 mutation which causes cystic fibrosis and its association with closely linked DNA polymorphisms in the Slovak population].
    Kádasi L, Gécz J, Puliti A, Devoto M, Ferák V, Romeo G, Kayserová H, Kardosová A, Hruskovic I.
    Bratisl Lek Listy; 1992 Mar 08; 93(3):141-5. PubMed ID: 1356071
    [Abstract] [Full Text] [Related]

  • 35. Cystic fibrosis gene variability in two southern Brazilian Amerindian populations: analysis of the deltaF508 mutation and the KM19 and XV2C haplotypes.
    Raskin S, Petzl-Erler ML, Phillips JA, Pereira-Ferrari L, Probst CM, Faucz FR, Sotomaior V, Salzano FM, Culpi L.
    Hum Biol; 2007 Feb 08; 79(1):79-91. PubMed ID: 17985657
    [Abstract] [Full Text] [Related]

  • 36. Association between haplotypes and specific mutations in Swiss cystic fibrosis families.
    Liechti-Gallati S, Malik N, Alkan M, Maechler M, Morris M, Thonney F, Sennhauser F, Moser H.
    Pediatr Res; 1991 Oct 08; 30(4):304-8. PubMed ID: 1683481
    [Abstract] [Full Text] [Related]

  • 37. Haplotype information and linkage disequilibrium mapping for single nucleotide polymorphisms.
    Lu X, Niu T, Liu JS.
    Genome Res; 2003 Sep 08; 13(9):2112-7. PubMed ID: 12952879
    [Abstract] [Full Text] [Related]

  • 38. Cystic fibrosis transmembrane regulator haplotypes in households of patients with cystic fibrosis.
    Furgeri DT, Marson FAL, Correia CAA, Ribeiro JD, Bertuzzo CS.
    Gene; 2018 Jan 30; 641():137-143. PubMed ID: 29054758
    [Abstract] [Full Text] [Related]

  • 39. Homogeneity of cystic fibrosis in Italy.
    Vitale E, Devoto M, Mastella G, Romeo G.
    Am J Hum Genet; 1986 Dec 30; 39(6):832-6. PubMed ID: 3467589
    [Abstract] [Full Text] [Related]

  • 40. Mild cystic fibrosis linked to chromosome 7q22 markers with an uncommon haplotype.
    McConkie-Rosell A, Chen YT, Harris D, Speer MC, Pericak-Vance MA, Ding JH, Highsmith WE, Knowles M, Kahler SG.
    Ann Intern Med; 1989 Nov 15; 111(10):797-801. PubMed ID: 2817627
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.