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Journal Abstract Search

170 related items for PubMed ID: 7515303

  • 1. 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; 3(2):141-51. PubMed ID: 7515303
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  • 7. 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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  • 8. A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis.
    Will K, Dörk T, Stuhrmann M, Meitinger T, Bertele-Harms R, Tümmler B, Schmidtke J.
    J Clin Invest; 1994 Apr; 93(4):1852-9. PubMed ID: 7512993
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  • 11. 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 Apr; 3(3):231-8. PubMed ID: 7517265
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  • 15. A frame-shift mutation in the cystic fibrosis gene.
    White MB, Amos J, Hsu JM, Gerrard B, Finn P, Dean M.
    Nature; 1990 Apr 12; 344(6267):665-7. PubMed ID: 1691449
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  • 18. Cystic fibrosis mutation frequencies in upstate New York.
    Shrimpton AE, Borowitz D, Swender P.
    Hum Mutat; 1997 Apr 12; 10(6):436-42. PubMed ID: 9401006
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  • 19. A 32-bp deletion (2991del32) in the cystic fibrosis gene associated with CFTR mRNA reduction.
    Dörk T, Will K, Grade K, Krawczak M, Tümmler B.
    Hum Mutat; 1994 Apr 12; 4(1):65-70. PubMed ID: 7524915
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  • 20. The study of cystic fibrosis transmembrane conductance regulator gene mutations in a group of patients from Romania.
    Frenţescu L, Brownsell E, Hinks J, Malone G, Shaw H, Budişan L, Bulman M, Schwarz M, Pop L, Filip M, Tomescu E, Moşescu S, Popa I, Benga G.
    J Cyst Fibros; 2008 Sep 12; 7(5):423-8. PubMed ID: 18467194
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