Search Results - van der Maarel, Sylvere M.

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    Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

    Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3 by Bitner-Glindzicz, Maria, Turnpenny, Peter, Höglund, Pia, Kääriäinen, Helena, Sankila, Eeva-Marja, van der Maarel, Sylvere M., de Kok, Yvette J.M., Ropers, Hans-Hilger, Cremers, Frans P.M., Pembrey, Marcus, Malcolm, Susan

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