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Journal Abstract Search

217 related items for PubMed ID: 7517264

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  • 5. 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
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  • 6. Single-stranded conformation polymorphism analysis of the CFTR gene in Slovenian cystic fibrosis patients: detection of mutations and sequence variations.
    Ravnik-Glavac M, Glavac D, Komel R, Dean M.
    Hum Mutat; 1993 Mar; 2(4):286-92. PubMed ID: 7691352
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  • 7. Four new mutations of the CFTR gene (541delC, R347H, R352Q, E585X) detected by DGGE analysis in Italian CF patients, associated with different clinical phenotypes.
    Cremonesi L, Ferrari M, Belloni E, Magnani C, Seia M, Ronchetto P, Rady M, Russo MP, Romeo G, Devoto M.
    Hum Mutat; 1992 Mar; 1(4):314-9. PubMed ID: 1284538
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  • 8. Screening for cystic fibrosis mutations in southern France: identification of a frameshift mutation and two missense variations.
    Claustres M, Gerrard B, Kjellberg P, Desgeorges M, Demaille J, Dean M.
    Hum Mutat; 1992 Mar; 1(4):310-3. PubMed ID: 1284537
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  • 10. Cystic fibrosis patients with mutation 1949del84 in exon 13 of the CFTR gene have a similar clinical severity as delta F508 homozygotes.
    Nunes V, Casals T, Gaona A, Antiñolo G, Ferrer-Calvete J, Pérez-Frias J, Tardío E, Molano J, Estivill X.
    Hum Mutat; 1992 Mar; 1(5):375-9. PubMed ID: 1284539
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  • 11. First study of CF mutations in the CFTR gene of Iranian patients: detection of DeltaF508, G542X, W1282X, A120T, R117H, and R347H mutations.
    Jalalirad M, Houshmand M, Mirfakhraie R, Goharbari MH, Mirzajani F.
    J Trop Pediatr; 2004 Dec; 50(6):359-61. PubMed ID: 15537723
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  • 14. 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
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  • 16. Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: identification of three novel alleles.
    Verlingue C, Kapranov NI, Mercier B, Ginter EK, Petrova NV, Audrezet MP, Férec C.
    Hum Mutat; 1995 Mar; 5(3):205-9. PubMed ID: 7541273
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  • 17. Identification of rare and novel mutations in the CFTR genes of CF patients in southern England.
    Shackleton S, Hull J, Dear S, Seller A, Thomson A, Harris A.
    Hum Mutat; 1994 Mar; 3(2):141-51. PubMed ID: 7515303
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  • 19. Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian population.
    Russo MP, Romeo G, Devoto M, Barbujani G, Cabrini G, Giunta A, D'Alcamo E, Leoni G, Sangiuolo F, Magnani C.
    Hum Mutat; 1995 Mar; 5(1):23-7. PubMed ID: 7537148
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  • 20. Prenatal diagnosis of cystic fibrosis in a highly heterogeneous population.
    Casals T, Gimenez J, Ramos MD, Nunes V, Estivill X.
    Prenat Diagn; 1996 Mar; 16(3):215-22. PubMed ID: 8710774
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