Results 271 to 280 of about 161,807 (290)

Contiguous deletion of SLC6A8 and BAP31 in a patient with severe dystonia and sensorineural deafness.

Molecular Genetics and Metabolism, 2012
H. Osaka, A. Takagi, Y. Tsuyusaki, T. Wada, M. Iai, S. Yamashita, Hiroko Shimbo, H. Saitsu, G. Salomons, C. Jakobs, N. Aida, Shinka Toshihiro, T. Kuhara, N. Matsumoto   +13 more
semanticscholar   +1 more source

The genetics of sensorineural deafness

Medical Journal of Australia, 1991
openaire   +2 more sources

Reversible sensori‐neural deafness

The Laryngoscope, 1960
F, KODMAN, O A, CULL, T O, LAWSON
openaire   +2 more sources

XXXV Sensorineural Deafness in Otosclerosis

Annals of Otology, Rhinology & Laryngology, 1966
J R, Lindsay, D D, Beal
openaire   +2 more sources

SENSORINEURAL DEAFNESS

1988
openaire   +1 more source

Sensorineural deafness following myringoplasty operations

The Journal of Laryngology & Otology, 1971
openaire   +2 more sources

CONGENITAL SENSORINEURAL DEAFNESS.

Texas state journal of medicine, 1996
B R, ALFORD, J R, DICKEY
openaire   +1 more source

Prevalence of sensorineural deafness in habitual mobile phone users

, 2011
G. Sahoo, Honeymol Sebastian
semanticscholar   +1 more source

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

Nature Genetics, 1999
F. Karet, K. Finberg, R. Nelson, A. Nayır, H. Mocan, S. Sanjad, J. Rodríguez-soriano, F. Santos, C. Cremers, A. Pietro, B. Hoffbrand, J. Winiarski, A. Bakkaloğlu, S. Ozen, R. Dusunsel, P. Goodyer, S. Hulton, Doris K. Wu, A. Skvorak, C. Morton, Michael J. Cunningham, Vivekanand Jha, R. Lifton   +22 more
semanticscholar   +1 more source

Connexin-26 mutations in sporadic and inherited sensorineural deafness

The Lancet, 1998
X. Estivill, P. Fortina, S. Surrey, R. Rabionet, S. Melchionda, L. D'agruma, E. Mansfield, E. Rappaport, N. Govea, Montse Milà, L. Zelante, P. Gasparini   +11 more
semanticscholar   +1 more source