Found: 11
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Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations.
- Published in:
- Human Genetics, 2002, v. 110, n. 5, p. 389, doi. 10.1007/s00439-002-0719-1
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- Article
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.
- Published in:
- Human Genetics, 2000, v. 107, n. 1, p. 7, doi. 10.1007/s004390050002
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- Article
Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment.
- Published in:
- Genes, 2020, v. 11, n. 6, p. 687, doi. 10.3390/genes11060687
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- Article
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNA<sup>Ser(UCN)</sup> gene.
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- European Journal of Human Genetics, 1999, v. 7, n. 1, p. 45, doi. 10.1038/sj.ejhg.5200247
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- Article
The Use of Malleus Allografts in Ossiculoplasty.
- Published in:
- Laryngoscope, 2002, v. 112, n. 10, p. 1782, doi. 10.1097/00005537-200210000-00014
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- Article
Transmeatal Procurement of Allograft Tympano-Ossicular Systems: Preliminary Report (Alternative to the intracranial bone plug technique by Schuknecht).
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- Journal of International Advanced Otology, 2012, v. 8, n. 2, p. 154
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- Article
A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis.
- Published in:
- Human Genetics, 2022, v. 141, n. 3/4, p. 951, doi. 10.1007/s00439-021-02334-8
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- Article
Risk Factors for Natural Hearing Evolution in Newborns With Congenital Cytomegalovirus Infection.
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- JAMA Otolaryngology-Head & Neck Surgery, 2024, v. 150, n. 1, p. 30, doi. 10.1001/jamaoto.2023.3507
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- Article
Risk Factors for Hearing Loss at Birth in Newborns With Congenital Cytomegalovirus Infection.
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- JAMA Otolaryngology-Head & Neck Surgery, 2023, v. 149, n. 2, p. 122, doi. 10.1001/jamaoto.2022.4109
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- Article
Insufficient evidence for a role of SERPINF1 in otosclerosis.
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- Molecular Genetics & Genomics, 2019, v. 294, n. 4, p. 1001, doi. 10.1007/s00438-019-01558-8
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- Article
Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 7, p. 1321, doi. 10.1093/hmg/8.7.1321
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- Article