Results 281 to 290 of about 139,963 (293)
Some of the next articles are maybe not open access.

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

Molecular Genetics and Metabolism, 2012
H. Osaka   +13 more
semanticscholar   +1 more source

XXXV Sensorineural Deafness in Otosclerosis

Annals of Otology, Rhinology & Laryngology, 1966
David D. Beal, John R. Lindsay
openaire   +3 more sources

XXXVIII Sensorineural Deafness and Otosclerosis

Annals of Otology, Rhinology & Laryngology, 1966
openaire   +2 more sources

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

Nature Genetics, 1999
F. Karet   +22 more
semanticscholar   +1 more source

XL Pathogenesis of Sensorineural Deafness in Otosclerosis

Annals of Otology, Rhinology & Laryngology, 1966
L. Rüedi, H. Spoendlin
openaire   +2 more sources

Connexin-26 mutations in sporadic and inherited sensorineural deafness

The Lancet, 1998
X. Estivill   +11 more
semanticscholar   +1 more source

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