APA

Van Laer L., Coucke P., Mueller R. F., Caethoven G., Flothmann K., Prasad S. D., Chamberlin G. P., Houseman M., Taylor G. R., Van de Heyning C. M., Fransen E., Rowland J., Cucci R. A., Smith R. J. & Van Camp G. (20011205). A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment. : Journal of medical genetics.

Chicago

Van Laer L, Coucke P, Mueller R F, Caethoven G, Flothmann K, Prasad S D, Chamberlin G P, Houseman M, Taylor G R, Van de Heyning C M, Fransen E, Rowland J, Cucci R A, Smith R J and Van Camp G. 20011205. A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment. : Journal of medical genetics.

Harvard

Van Laer L., Coucke P., Mueller R. F., Caethoven G., Flothmann K., Prasad S. D., Chamberlin G. P., Houseman M., Taylor G. R., Van de Heyning C. M., Fransen E., Rowland J., Cucci R. A., Smith R. J. and Van Camp G. (20011205). A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment. : Journal of medical genetics.

MLA

Van Laer L, Coucke P, Mueller R F, Caethoven G, Flothmann K, Prasad S D, Chamberlin G P, Houseman M, Taylor G R, Van de Heyning C M, Fransen E, Rowland J, Cucci R A, Smith R J and Van Camp G. A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment. : Journal of medical genetics. 20011205.