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Published in The European respiratory journal (01.01.2010)
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Systemic impairment in relation to disease burden in patients with moderate COPD eligible for a lifestyle program. Findings from the INTERCOM trial
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Published in International journal of chronic obstructive pulmonary disease (2008)
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Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene
van de Wetering, R.A.C, Gabreëls-Festen, A.A.W.M, Timmerman, V, Padberg, G.W, Gabreëls, F.J.M, Mariman, E.C.M
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Assignment of the human gene for receptor-type protein tyrosine phosphatase IA-2 (PTPRN) to chromosome region 2q35→q36.1 and identification of an intragenic genetic marker
VAN DEN MAAGDENBERG, A. M. J. M, WEGHUIS, D. O, RIJSS, J, VAN DE WETERING, R. A. C, WIERINGA, B, VAN KESSEL, A. G, HENDRIKS, W. J. A. J
Published in Cytogenetic and genome research (01.01.1996)
Published in Cytogenetic and genome research (01.01.1996)
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