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Journal Abstract Search

507 related items for PubMed ID: 11924117

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  • 2. Geographic distribution of cystic fibrosis transmembrane regulator gene mutations in Saudi Arabia.
    Banjar H, Kambouris M, Meyer BF, al-Mehaidib A, Mogarri I.
    Ann Trop Paediatr; 1999 Mar; 19(1):69-73. PubMed ID: 10605524
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  • 4. [Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].
    Iwańczak F, Smigiel R, Stawarski A, Pawłowicz J, Stembalska A, Mowszet K, Sasiadek M.
    Pol Merkur Lekarski; 2005 Feb; 18(104):205-9. PubMed ID: 17877132
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  • 8. Genotype-phenotype relationship for five CFTR mutations frequently identified in western France.
    Duguépéroux I, De Braekeleer M, Participating Centres to the French National Cystic Fibrosis Registry.
    J Cyst Fibros; 2004 Dec; 3(4):259-63. PubMed ID: 15698945
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  • 9. Cystic fibrosis mutations with widely variable phenotype: the D1152H example.
    Mussaffi H, Prais D, Mei-Zahav M, Blau H.
    Pediatr Pulmonol; 2006 Mar; 41(3):250-4. PubMed ID: 16429425
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  • 14. [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
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  • 15. [An analysis of the mutations in the mucoviscidosis gene: the origin and distribution of the delF508 major mutation in Ukraine].
    Livshits LA, Kravchenko SA, Musienko SI, Maliarchuk SG.
    Tsitol Genet; 1995 Feb 24; 29(6):67-73. PubMed ID: 8713839
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  • 19. 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 24; 7(2):110-5. PubMed ID: 17716958
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  • 20. [Cystic fibrosis: the CFTR gene, its mutations, the genetic counseling].
    Goossens M, Ghanem N, Girodon E, Costes B, Fanen P.
    Rev Pneumol Clin; 1995 Mar 24; 51(3):130-6. PubMed ID: 7569574
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