Found: 11
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Spatiotemporal expression patterns of clusterin in the mouse inner ear.
- Published in:
- Cell & Tissue Research, 2017, v. 370, n. 1, p. 89, doi. 10.1007/s00441-017-2650-8
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- Article
Multiplex minisequencing screening for PTC genotype associated with bitter taste perception.
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- Molecular Biology Reports, 2014, v. 41, n. 3, p. 1563, doi. 10.1007/s11033-013-3002-8
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- Article
Identiication of Causative Mutation in a Korean Family with Crouzon Syndrome Using Whole Exome Sequencing.
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- Annals of Clinical & Laboratory Science, 2014, v. 44, n. 4, p. 476
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- Article
Evaluation of the Contribution of the EYA4 and GRHL2 Genes in Korean Patients with Autosomal Dominant Non-Syndromic Hearing Loss.
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- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0119443
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- Article
Genetic Analysis of Genes Related to Tight Junction Function in the Korean Population with Non-Syndromic Hearing Loss.
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- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0095646
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- Article
A Rapid Method for Simultaneous Screening of Multi-Gene Mutations Associated with Hearing Loss in the Korean Population.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0057237
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- Article
A novel missense variant in the DIAPH1 gene in a Korean family with autosomal dominant nonsyndromic hearing loss.
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- Genes & Genetic Systems, 2016, v. 91, n. 5, p. 289, doi. 10.1266/ggs.16-00041
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- Article
A mutation of the succinate dehydrogenase B gene in a Korean family with paraganglioma.
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- Familial Cancer, 2016, v. 15, n. 4, p. 601, doi. 10.1007/s10689-016-9874-8
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- Article
A Systematic Survey of Carbonic Anhydrase mRNA Expression During Mammalian Inner Ear Development.
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- Developmental Dynamics, 2013, v. 242, n. 3, p. 269, doi. 10.1002/dvdy.23917
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- Article
Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans.
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- BMC Medical Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12881-016-0269-3
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- Article
Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families.
- Published in:
- BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-72
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- Article