APA

Hildebrand M. S., Thorne N. P., Bromhead C. J., Kahrizi K., Webster J. A., Fattahi Z., Bataejad M., Kimberling W. J., Stephan D., Najmabadi H., Bahlo M. & Smith R. J. H. (20101005). Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation. : Clinical genetics.

Chicago

Hildebrand M S, Thorne N P, Bromhead C J, Kahrizi K, Webster J A, Fattahi Z, Bataejad M, Kimberling W J, Stephan D, Najmabadi H, Bahlo M and Smith R J H. 20101005. Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation. : Clinical genetics.

Harvard

Hildebrand M. S., Thorne N. P., Bromhead C. J., Kahrizi K., Webster J. A., Fattahi Z., Bataejad M., Kimberling W. J., Stephan D., Najmabadi H., Bahlo M. and Smith R. J. H. (20101005). Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation. : Clinical genetics.

MLA

Hildebrand M S, Thorne N P, Bromhead C J, Kahrizi K, Webster J A, Fattahi Z, Bataejad M, Kimberling W J, Stephan D, Najmabadi H, Bahlo M and Smith R J H. Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation. : Clinical genetics. 20101005.