Search Results - "Kaspers, A G"

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  1. 1
    Compound SFTPB 1549C→GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency

    Compound SFTPB 1549C→GAA (121ins2) and 457delC heterozygosity in severe congenital lung disease and surfactant protein B (SP-B) deficiency by Tredano, Mohammed, van Elburg, Ruurd M., Kaspers, Ageeth G., Zimmermann, Luc J., Houdayer, Claude, Aymard, Pierre, Hull, William M., Whitsett, Jeffrey A., Elion, Jacques, Griese, Matthias, Bahuau, Michel

    Published in Human mutation (01-01-1999)
    “…Several human respiratory disorders have been linked to an abnormality of pulmonary surfactant synthesis or turnover. Among those conditions, hereditary…”
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  2. 2
    Compound SFTPB 1549C arrow right GAA (121ins2) and 457delC Heterozygosity in Severe Congenital Lung Disease and Surfactant Protein B (SP-B) Deficiency

    Compound SFTPB 1549C arrow right GAA (121ins2) and 457delC Heterozygosity in Severe Congenital Lung Disease and Surfactant Protein B (SP-B) Deficiency by Tredano, M, Van Elburg, RM, Kaspers, A G, Zimmermann, L J, Houdayer, C, Aymard, P, Hull, WM, Whitsett, JA, Elion, J, Griese, M, Bahuau, M

    Published in Human mutation (01-01-1999)
    “…Several human respiratory disorders have been linked to an abnormality of pulmonary surfactant synthesis or turnover. Among those conditions, hereditary…”
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    Journal Article
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