Cite
HARVARD Citation
Van Laer, L. et al. (2001). A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment. Journal of medical genetics. 38 (8), pp. 515-518. [Online].
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Van Laer, L. et al. (2001). A common founder for the 35delG GJB2gene mutation in connexin 26 hearing impairment. Journal of medical genetics. 38 (8), pp. 515-518. [Online].