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Panel 3: Genetics and Precision Medicine of Otitis Media.
- Published in:
- 2017
- By:
- Publication type:
- journal article
A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis.
- Published in:
- Journal of Bone & Mineral Research, 2003, v. 18, n. 9, p. 1612, doi. 10.1359/jbmr.2003.18.9.1612
- By:
- Publication type:
- Article
A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice.
- Published in:
- Nature Genetics, 2001, v. 27, n. 2, p. 191, doi. 10.1038/84831
- By:
- Publication type:
- Article
Mouse mutants from chemically mutagenized embryonic stem cells.
- Published in:
- Nature Genetics, 2000, v. 24, n. 3, p. 318, doi. 10.1038/73563
- By:
- Publication type:
- Article
Sh3pxd2b Mice Are a Model for Craniofacial Dysmorphology and Otitis Media.
- Published in:
- PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0022622
- By:
- Publication type:
- Article
Prevalence of cytomegalovirus carriage among childcare staff.
- Published in:
- 2017
- By:
- Publication type:
- Letter
The roles of USH1 proteins and PDZ domain-containing USH proteins in USH2 complex integrity in cochlear hair cells.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 3, p. 624, doi. 10.1093/hmg/ddw421
- By:
- Publication type:
- Article
Otitis media in a mouse model for Down syndrome.
- Published in:
- International Journal of Experimental Pathology, 2009, v. 90, n. 5, p. 480, doi. 10.1111/j.1365-2613.2009.00677.x
- By:
- Publication type:
- Article
Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in usher syndrome type 1F.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 8, p. 1515, doi. 10.1093/hmg/ddq025
- By:
- Publication type:
- Article