Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis von Oonk, A.M.M., Leijendeckers, J.M., Lammers, E.M., Weegerink, N.J.D., Oostrik, J., Beynon, A.J., Huygen, P.L.M., Kunst, H.P.M., Kremer, H., Snik, A.F.M., Pennings, R.J.E.

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Audiometric characteristics of two Dutch families with non-ocular Stickler syndrome (COL11A2) von van Beelen, E., Leijendeckers, J.M., Huygen, P.L.M., Admiraal, R.J.C., Hoefsloot, L.H., Lichtenbelt, K.D., Stöbe, L., Pennings, R.J.E., Leuwer, R., Snik, A.F.M., Kunst, H.P.M.

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Audiometric Characteristics of a Dutch Family with a New Mutation in GATA3 Causing HDR Syndrome von van Beelen, E., Leijendeckers, J.M., Admiraal, R.J.C., Huygen, P.L.M., Hoefsloot, L.H., Pennings, R.J.E., Snik, A.F.M., Kunst, H.P.M.

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