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

151 related items for PubMed ID: 12938099

  • 1. CFTR mutations in patients from Colombia: implications for local and regional molecular diagnosis programs.
    Keyeux G, Rodas C, Bienvenu T, Garavito P, Vidaud D, Sanchez D, Kaplan JC, Aristizábal G.
    Hum Mutat; 2003 Sep; 22(3):259. PubMed ID: 12938099
    [Abstract] [Full Text] [Related]

  • 2. High heterogeneity of CFTR mutations and unexpected low incidence of cystic fibrosis in the Mediterranean France.
    des Georges M, Guittard C, Altiéri JP, Templin C, Sarles J, Sarda P, Claustres M.
    J Cyst Fibros; 2004 Dec; 3(4):265-72. PubMed ID: 15698946
    [Abstract] [Full Text] [Related]

  • 3. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
    [Abstract] [Full Text] [Related]

  • 4. 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; 71(Pt 2):194-201. PubMed ID: 17331079
    [Abstract] [Full Text] [Related]

  • 5. Characterisation of mutations and genotype-phenotype correlation in cystic fibrosis: experience from India.
    Shastri SS, Kabra M, Kabra SK, Pandey RM, Menon PS.
    J Cyst Fibros; 2008 Mar; 7(2):110-5. PubMed ID: 17716958
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations.
    Kinnunen S, Bonache S, Casals T, Monto S, Savilahti E, Kere J, Järvelä I.
    J Cyst Fibros; 2005 Dec; 4(4):233-7. PubMed ID: 16051530
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. 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]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Mutation analysis of CFTR gene in 70 Iranian cystic fibrosis patients.
    Alibakhshi R, Zamani M.
    Iran J Allergy Asthma Immunol; 2006 Mar; 5(1):3-8. PubMed ID: 17242497
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [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]

    Page: [Next] [New Search]
    of 8.