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

103 related items for PubMed ID: 8890528

  • 21. CFTR mutations in the Algerian population.
    Loumi O, Ferec C, Mercier B, Creff J, Fercot B, Denine R, Grangaud JP.
    J Cyst Fibros; 2008 Jan; 7(1):54-9. PubMed ID: 17572159
    [Abstract] [Full Text] [Related]

  • 22. [Detection of frequent mutations of the CFTR gene in cystic fibrosis patients from Central Russia].
    Petrova NV, Kapranov NI, Ginter EK.
    Genetika; 1997 Jan; 33(1):106-9. PubMed ID: 9162681
    [Abstract] [Full Text] [Related]

  • 23. [Identification of mutation in the gene cystic fibrosis transmembrane regulator (CFTR) in Chilean patients with cystic fibrosis].
    Repetto G, Poggi H, Harris P, Navarro H, Sánchez I, Guiraldes E, Pérez MA, Boza ML, Hunter B, Wevar ME, Mediavilla M, Foradori A.
    Rev Med Chil; 2001 Aug; 129(8):841-7. PubMed ID: 11680956
    [Abstract] [Full Text] [Related]

  • 24. Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles.
    Faucz FR, Gimenez J, Ramos MD, Pereira-Ferrari L, Estivill X, Raskin S, Casals T, Culpi L.
    Clin Genet; 2007 Sep; 72(3):218-23. PubMed ID: 17718859
    [Abstract] [Full Text] [Related]

  • 25. A novel donor splice site characterized by CFTR mRNA analysis induces a new pseudo-exon in CF patients.
    Costantino L, Claut L, Paracchini V, Coviello DA, Colombo C, Porcaro L, Capasso P, Zanardelli M, Pizzamiglio G, Degiorgio D, Seia M.
    J Cyst Fibros; 2010 Dec; 9(6):411-8. PubMed ID: 20875776
    [Abstract] [Full Text] [Related]

  • 26. A 96-well formatted method for exon and exon/intron boundary full sequencing of the CFTR gene.
    Lucarelli M, Narzi L, Piergentili R, Ferraguti G, Grandoni F, Quattrucci S, Strom R.
    Anal Biochem; 2006 Jun 15; 353(2):226-35. PubMed ID: 16635477
    [Abstract] [Full Text] [Related]

  • 27. Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controls.
    Weiss FU, Simon P, Bogdanova N, Mayerle J, Dworniczak B, Horst J, Lerch MM.
    Gut; 2005 Oct 15; 54(10):1456-60. PubMed ID: 15987793
    [Abstract] [Full Text] [Related]

  • 28. Identification of a novel mutation of CFTR gene in a Korean patient with cystic fibrosis.
    Ko JM, Kim GH, Kim KM, Hong SJ, Yoo HW.
    J Korean Med Sci; 2008 Oct 15; 23(5):912-5. PubMed ID: 18955805
    [Abstract] [Full Text] [Related]

  • 29. High incidence of the CFTR mutations 3272-26A-->G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A-->G, E588V, and 1671insTATCA).
    Storm K, Moens E, Vits L, De Vlieger H, Delaere G, D'Hollander M, Wuyts W, Biervliet M, Van Schil L, Desager K, Nöthen MM.
    J Cyst Fibros; 2007 Nov 30; 6(6):371-5. PubMed ID: 17481968
    [Abstract] [Full Text] [Related]

  • 30. DHPLC screening of cystic fibrosis gene mutations.
    Ravnik-Glavac M, Atkinson A, Glavac D, Dean M.
    Hum Mutat; 2002 Apr 30; 19(4):374-83. PubMed ID: 11933191
    [Abstract] [Full Text] [Related]

  • 31. [TUB9 polymorphism in the CFTR gene of cystic fibrosis patients, carriers, and healthy donors from the Moscow region. SSCP and restriction analyses].
    Amosenko FA, Trubnikova IS, Zakhar'ev VM, Bannikov VM, Sazonova MA, Petrova NV, Kapranov NI, Kaplinin VN.
    Genetika; 1997 Feb 30; 33(2):257-61. PubMed ID: 9162703
    [Abstract] [Full Text] [Related]

  • 32. Two novel missense and one novel nonsense CFTR mutations in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R, Gourabi H, Gilani MA, Dizaj AV, Rezaee M, Mollamohamadi S.
    Mol Hum Reprod; 2006 Nov 30; 12(11):717-21. PubMed ID: 16973827
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry.
    Alonso MJ, Heine-Suñer D, Calvo M, Rosell J, Giménez J, Ramos MD, Telleria JJ, Palacio A, Estivill X, Casals T.
    Ann Hum Genet; 2007 Mar 30; 71(Pt 2):194-201. PubMed ID: 17331079
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. [Cystic fibrosis transmembrane conductance regulator (CFTR) gene: mutations and clinical phenotypes].
    Schwartz M.
    Ugeskr Laeger; 2003 Feb 24; 165(9):912-6. PubMed ID: 12661515
    [Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 6.