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Authors: Tredano, M Cneude, F Denamur, E Truffert, P Capron, F Manouvrier, S Feldmann, D Couderc, R Elion, J Lacaze-Masmonteil, T

Citation: M. Tredano et al., Clinical presentation, immunohistologic features, molecular confirmation, and prenatal diagnosis of surfactant protein B (SP-B) deficiency., ARCH PED, 7(6), 2000, pp. 641-644

Authors: Houdayer, C Lemonnier, A Gerard, M Chauve, C Tredano, M de Villemeur, TB Aymard, P Bonnefont, JP Feldmann, D

Citation: C. Houdayer et al., Improved fluorescent PCR-based assay for sizing CGG repeats at the FRAXA locus, CLIN CH L M, 37(4), 1999, pp. 397-401

Authors: Tredano, M van Elburg, RM Kaspers, AG Zimmermann, LJ Houdayer, C Aymard, P Hull, WM Whitsett, JA Elion, J Griese, M Bahuau, M

Citation: M. Tredano et al., Compound SFTPB 1549C -> GAA (121ins2) and 457delC heterozygosity in severecongenital lung disease and surfactant protein B (SP-B) deficiency, HUM MUTAT, 14(6), 1999, pp. 502-509

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Citation: C. Houdayer et al., Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait, ANN GENET, 42(2), 1999, pp. 69-74