Found: 6
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Temporal Bone Histopathological and Quantitative Analysis of Mitochondrial DNA in MELAS.
- Published in:
- Laryngoscope, 2003, v. 113, n. 8, p. 1362
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- Publication type:
- Article
Nonsyndromic Hearing Loss Caused by a Mitochondrial T7511C Mutation.
- Published in:
- Laryngoscope, 2002, v. 112, n. 8, p. 1494, doi. 10.1097/00005537-200208000-00030
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- Publication type:
- Article
Phenotype of DFNA11: A Nonsyndromic Hearing Loss Caused by a Myosin VIIA Mutation.
- Published in:
- Laryngoscope, 2002, v. 112, n. 2, p. 292, doi. 10.1097/00005537-200202000-00017
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- Publication type:
- Article
Hereditary sensorineural hearing loss of unknown cause involving mitochondrial DNA 1555 mutation.
- Published in:
- 2000
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- Publication type:
- journal article
A new mutation in the POU3F4 gene in a japanese family with x-linked mixed deafness (DFN3).
- Published in:
- Laryngoscope, 1998, v. 108, n. 10, p. 1544, doi. 10.1097/00005537-199810000-00022
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- Publication type:
- Article
A Gene for a Dominant Form of Non-Syndromic Sensorineural Deafness (DFNA11) Maps Within the Region Containing the DFNB2 Recessive Deafness Gene.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 6, p. 849, doi. 10.1093/hmg/5.6.849
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- Publication type:
- Article