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  1. 1
    A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome

    A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome von de Zwart-Storm, E.A., van Geel, M., Veysey, E., Burge, S., Cooper, S., Steijlen, P.M., Martin, P.E., van Steensel, M.A.M.


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  2. 2
    Skin changes in oculo‐dento‐digital dysplasia are correlated with C‐terminal truncations of connexin 43

    Skin changes in oculo‐dento‐digital dysplasia are correlated with C‐terminal truncations of connexin 43 von Vreeburg, M., de Zwart‐Storm, E.A., Schouten, M.I., Nellen, R.G.L., Marcus‐Soekarman, D., Devies, M., van Geel, M., van Steensel, M.A.M.


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  3. 3
    A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome: A novel mutation in GJB2 causes Vohwinkel syndrome

    A novel missense mutation in GJB2, p.Tyr65His, causes severe Vohwinkel syndrome: A novel mutation in GJB2 causes Vohwinkel syndrome von de Zwart-Storm, E.A., van Geel, M., Veysey, E., Burge, S., Cooper, S., Steijlen, P.M., Martin, P.E., van Steensel, M.A.M.


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  4. 4
    Skin changes in oculo-dento-digital dysplasia are correlated with C-terminal truncations of connexin 43

    Skin changes in oculo-dento-digital dysplasia are correlated with C-terminal truncations of connexin 43 von Vreeburg, M., de Zwart-Storm, E.A., Schouten, M.I., Nellen, R.G.L., Marcus-Soekarman, D., Devies, M., van Geel, M., van Steensel, M.A.M.


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