APA

Kalay E., Karaguzel A., Caylan R., Heister A., Cremers F. P. M., Cremers C. W. R. J., Brunner H. G., de Brouwer A. P. M. & Kremer H. (20060613). Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss. : Human mutation.

Chicago

Kalay E, Karaguzel A, Caylan R, Heister A, Cremers F P M, Cremers C W R J, Brunner H G, de Brouwer A P M and Kremer H. 20060613. Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss. : Human mutation.

Harvard

Kalay E., Karaguzel A., Caylan R., Heister A., Cremers F. P. M., Cremers C. W. R. J., Brunner H. G., de Brouwer A. P. M. and Kremer H. (20060613). Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss. : Human mutation.

MLA

Kalay E, Karaguzel A, Caylan R, Heister A, Cremers F P M, Cremers C W R J, Brunner H G, de Brouwer A P M and Kremer H. Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss. : Human mutation. 20060613.