Results 211 to 220 of about 161,807 (290)

Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)

open access: yesEuropean Journal of Human Genetics, 2009
O. Alsmadi   +7 more
semanticscholar   +1 more source

Unilateral and bilateral congenital sensorineural deafness in client-owned pure-breed white cats.

open access: yesJournal of Veterinary Internal Medicine, 2009
D. Cvejić   +3 more
semanticscholar   +1 more source

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