Results 221 to 230 of about 31,332 (279)

Cochlear implantation in children with Bartter syndrome: A case report. [PDF]

open access: yesSci Prog
Badr KM   +5 more
europepmc   +1 more source

Audiological findings in Brown Vialetto-Van-Laere Syndrome: A scoping review. [PDF]

open access: yesBraz J Otorhinolaryngol
Rolim DO   +5 more
europepmc   +1 more source

Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy

open access: green, 2017
Rajech Sharkia   +13 more
openalex   +2 more sources

Dominant ER Stress–Inducing WFS1 Mutations Underlie a Genetic Syndrome of Neonatal/Infancy-Onset Diabetes, Congenital Sensorineural Deafness, and Congenital Cataracts

open access: bronze, 2017
Elisa De Franco   +15 more
openalex   +1 more source

The audiological phenotype of patients with a variant in MYH9 and MYH14 genes. [PDF]

open access: yesSci Rep
Bae SH   +7 more
europepmc   +1 more source

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