PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspring von Hellebrekers, D M E I, Wolfe, R, Hendrickx, A T M, de Coo, I F M, de Die, C E, Geraedts, J P M, Chinnery, P F, Smeets, H J M

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MTO01 Chip-based MtDNA mutation screening enables fast and reliable genetic diagnosis of oxphos patients von de Coo, R.I.F.M, Gerards, M, van Eijsden, R.G.E, Hendrickx, A.T.M, Stassen, F, Rubio-Gozalbo, M.E, Tiranti, V, Smeets, H.J.M

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Inherited mitochondrial variants are not a major cause of age-related hearing impairment in the European population von Bonneux, S, Fransen, E, Van Eyken, E, Van Laer, L, Huyghe, J, Van de Heyning, P, Voets, A, Gerards, M, Stassen, A P M, Hendrickx, A T M, Smeets, H J M, Van Camp, G

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Additional mitochondrial DNA mutations may explain extra-ocular involvement in LHON von Spruijt, L., Hoogendijk, J.E., Hendrickx, A.T.M., de Coo, I.F., Doevendans, P.A., de Jong, P.T.V.M., Spliet, W.G.M., Kroes, H., Smeets, H.J.

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Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNA Leu(UUR) gene von van den Bosch, B.J.C., de Coo, I.F.M., Hendrickx, A.T.M., Busch, H.F.M., de Jong, G., Scholte, H.R., Smeets, H.J.M.

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Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) gene von van den Bosch, B J C, de Coo, I F M, Hendrickx, A T M, Busch, H F M, de Jong, G, Scholte, H R, Smeets, H J M

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Nuclear import as a barrier to infection of human umbilical vein endothelial cells by human cytomegalovirus strain AD169 von Slobbe-van Drunen, M.E.P, Hendrickx, A.T.M, Vossen, R.C.R.M, Speel, E.J.M, van Dam-Mieras, M.C.E, Bruggeman, C.A

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