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PUBMED FOR HANDHELDS

Journal Abstract Search


95 related items for PubMed ID: 18258563

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  • 5. Clinical characterization and diagnosis of cystic fibrosis through exome sequencing in Chinese infants with Bartter-syndrome-like hypokalemia alkalosis.
    Qiu L, Yang F, He Y, Yuan H, Zhou J.
    Front Med; 2018 Oct; 12(5):550-558. PubMed ID: 29520692
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  • 9. Bartter syndrome with long-term follow-up: a case report.
    Wu X, Yang G, Chen S, Tang M, Jian S, Chen F, Wu X.
    J Int Med Res; 2020 Aug; 48(8):300060520947876. PubMed ID: 32857947
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  • 10. Identification of a novel mutation (S13F) in the CFTR gene in a CF patient of Sardinian origin.
    Leoni GB, Pitzalis S, Tonelli R, Cao A.
    Hum Mutat; 1998 Aug; 11(4):337. PubMed ID: 9554753
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  • 11. 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 Aug; 1(5):375-9. PubMed ID: 1284539
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