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    Article

    Camurati–Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family

    We report on a 46-year-old mother of Moroccan origin, suffering mainly from painful, swollen legs, and her 26-year-old son who had experienced intense pain in his legs, without fever, for approximately 3 years...

    S. Simsek, K. Janssens, M. L. Kwee, W. Van Hul, J. Veenstra… in Osteoporosis International (2005)

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    Unusual response to bifunctional alkylating agents in a case of Fanconi anaemia

    Chromosomal breakage frequencies were determined in Fanconi anaemia (FA) blood cultures treated with various concentrations of the polyfunctional alkylating agents mitomycin C, diepoxybutane, and cis-platinum(II)...

    M. L. Kwee, E. H. A. Poll, J. J. P. van de Kamp, H. de Koning… in Human Genetics (1983)