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Journal Abstract Search

154 related items for PubMed ID: 7524914

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  • 3. Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR.
    Feriotto G, Ferlini A, Ravani A, Calzolari E, Mischiati C, Bianchi N, Gambari R.
    Hum Mutat; 2001; 18(1):70-81. PubMed ID: 11438995
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  • 4. Screening for CF mutations in adult cystic fibrosis patients with a directed and optimized SSCP strategy.
    Ravnik-Glavac M, Glavac D, Chernick M, di Sant'Agnese P, Dean M.
    Hum Mutat; 1994; 3(3):231-8. PubMed ID: 7517265
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  • 5. Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
    Zielenski J, Markiewicz D, Chen HS, Schappert K, Seller A, Durie P, Corey M, Tsui LC.
    Hum Mutat; 1995; 5(1):43-7. PubMed ID: 7537150
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  • 6. Identification of the commonest cystic fibrosis transmembrane regulator gene DeltaF508 mutation: evaluation of PCR--single-strand conformational polymorphism and polyacrylamide gel electrophoresis.
    Kakavas KV, Noulas AV, Kanakis I, Bonanou S, Karamanos NK.
    Biomed Chromatogr; 2006 Oct; 20(10):1120-5. PubMed ID: 16708396
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  • 7. 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 Oct; 1(4):310-3. PubMed ID: 1284537
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  • 10. Identification of a new splicing mutation (406-1 G-C) in the CFTR gene.
    Bonizzato A, Nicolis E, Gasparini P.
    Hum Mutat; 1992 Oct; 1(5):432-3. PubMed ID: 1284541
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  • 11. DHPLC screening of cystic fibrosis gene mutations.
    Ravnik-Glavac M, Atkinson A, Glavac D, Dean M.
    Hum Mutat; 2002 Apr; 19(4):374-83. PubMed ID: 11933191
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  • 13. Non radioactive single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene using the Pharmacia PhastSystem.
    Cormier-Daire V, Clavel C, Polette M, Doco M, Boutterin MC, Binninger I, Birembaut P.
    Pathol Biol (Paris); 1993 Oct; 41(8):713-5. PubMed ID: 8290318
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  • 14. Multiple fluorescence-based PCR-SSCP analysis.
    Iwahana H, Yoshimoto K, Mizusawa N, Kudo E, Itakura M.
    Biotechniques; 1994 Feb; 16(2):296-7, 300-5. PubMed ID: 8179893
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  • 15. Simultaneous detection of the two prevalent mutations in the cystic fibrosis gene in Reunion Island.
    Bienvenu T, Bousquet S, Herbulot C, Cartault F, Kaplan JC, Beldjord C.
    Hum Mutat; 1993 Feb; 2(4):306-8. PubMed ID: 7691353
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  • 17. A rapid, efficient, and sensitive assay for simultaneous detection of multiple cystic fibrosis mutations.
    Costes B, Fanen P, Goossens M, Ghanem N.
    Hum Mutat; 1993 Feb; 2(3):185-91. PubMed ID: 7689902
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  • 18. 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
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  • 19. [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; 33(2):257-61. PubMed ID: 9162703
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  • 20. Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease.
    Liechti-Gallati S, Schneider V, Neeser D, Kraemer R.
    Eur J Hum Genet; 1999 Jul; 7(5):590-8. PubMed ID: 10439967
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