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Searching for the Molecular Basis of Partial Deafness.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 11, p. 6029, doi. 10.3390/ijms23116029
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- Article
Update on CD164 and LMX1A genes to strengthen their causative role in autosomal dominant hearing loss.
- Published in:
- Human Genetics, 2022, v. 141, n. 3/4, p. 445, doi. 10.1007/s00439-022-02443-y
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- Article
POSTLINGUAL SENSORINEURAL HEARING LOSS DUE TO A KNOWN TBC1D24 GENE ALTERATION.
- Published in:
- Journal of Hearing Science, 2021, v. 11, n. 4, p. 72, doi. 10.17430/JHS.2021.11.4.8
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- Article
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation.
- Published in:
- Genes, 2023, v. 14, n. 2, p. 335, doi. 10.3390/genes14020335
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- Publication type:
- Article
Complex Phenotypic Presentation of Syndromic Hearing Loss Deciphered as Three Separate Clinical Entities: How Genetic Testing Guides Final Diagnosis.
- Published in:
- Audiology & Neurotology, 2021, v. 26, n. 4, p. 226, doi. 10.1159/000510695
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- Article