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Early audiological phenotype in patients with mutations in the USH2A gene
by
Markova, T.G.
,
Lalayants, M.R.
,
Alekseeva, N.N.
,
Ryzhkova, O.P.
,
Shatokhina, O.L.
,
Galeeva, N.M.
,
Bliznetz, E.A.
,
Weener, M.E.
,
Belov, O.A.
,
Chibisova, S.S.
,
Polyakov, A.V.
,
Tavartkiladze, G.A.
Published in
International journal of pediatric otorhinolaryngology
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International Journal Of Pediatric Otorhinolaryngology
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Audiometry
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Child
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Congenital Mild-To-Moderate Nonsyndromic Sensorineural Hearing Loss
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Extracellular Matrix Proteins - Genetics
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Gjb2
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Hearing Loss, Sensorineural - Diagnosis
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Hearing Loss, Sensorineural - Genetics
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Humans
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Intercellular Signaling Peptides And Proteins - Genetics
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Life Sciences & Biomedicine
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Mutation
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Otorhinolaryngology
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Pediatrics
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Phenotype
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Retinitis Pigmentosa
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Science & Technology
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Strc Genes
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Universal Newborn Hearing Screening
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Ush2A
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Usher Syndrome Type Ii
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Sciencedirect (Online Service)
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Sciencedirect Freedom Collection 2022-2024
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