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Results: 80,428
Number of items: 80,428
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Wilcox, W. R., Banikazemi, M., Guffon, N., Waldek, S., Lee, P., Linthorst, G. E., Desnick, R. J., & Germain, D. P. (2004). Long-term safety and efficacy of enzyme replacement therapy for Fabry disease. American Journal of Human Genetics, 75(1), 65-74. https://doi.org/10.1086/422366 -
Matera, I., Bachetti, T., Puppo, F., Duca, M., Morandi, F., Casiraghi, G. M., Cilio, M. R., Hennekam, R. C. M., Hofstra, R., Schöber, J. G., Ravazzolo, R., Ottonello, G., & Ceccherini, I. (2004). PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome. Journal of Medical Genetics, 41(5), 373-380. -
Di Cocco, G., Foschini, L., Grandi, P., Malaguti, G., Castro-Tirado, A. J., Chaty, S., Dean, A. J., Gehrels, N., Grenier, I., Hermsen, W., Kuiper, L., Lund, N., & Mirabel, F. (2004). INTEGRAL observation of 3EG J1736-2908. Astronomy & Astrophysics, 425, 89-93. https://doi.org/10.1051/0004-6361:20040484
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