Found: 4
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Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families.
- Published in:
- 2008
- By:
- Publication type:
- Letter
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese family.
- Published in:
- Clinical Genetics, 2007, v. 72, n. 5, p. 471, doi. 10.1111/j.1399-0004.2007.00889.x
- By:
- Publication type:
- Article
Improving Corrosion Resistance of Ferrous Alloy to Molten Zn by Modifying the Laves Phase Characteristics.
- Published in:
- JOM: The Journal of The Minerals, Metals & Materials Society (TMS), 2018, v. 70, n. 11, p. 2457, doi. 10.1007/s11837-017-2493-5
- By:
- Publication type:
- Article
Phase Equilibria of the Fe-Mo-Ta Ternary System.
- Published in:
- Journal of Phase Equilibria & Diffusion, 2019, v. 40, n. 3, p. 413, doi. 10.1007/s11669-019-00738-8
- By:
- Publication type:
- Article