APA

Lench N. J., Markham A. F., Mueller R. F., Kelsell D. P., Smith R. J., Willems P. J., Schatteman I., Capon H., Van De Heyning P. J. & Van Camp G. (19980423). A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2). : Journal of medical genetics.

Chicago

Lench N J, Markham A F, Mueller R F, Kelsell D P, Smith R J, Willems P J, Schatteman I, Capon H, Van De Heyning P J and Van Camp G. 19980423. A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2). : Journal of medical genetics.

Harvard

Lench N. J., Markham A. F., Mueller R. F., Kelsell D. P., Smith R. J., Willems P. J., Schatteman I., Capon H., Van De Heyning P. J. and Van Camp G. (19980423). A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2). : Journal of medical genetics.

MLA

Lench N J, Markham A F, Mueller R F, Kelsell D P, Smith R J, Willems P J, Schatteman I, Capon H, Van De Heyning P J and Van Camp G. A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2). : Journal of medical genetics. 19980423.