Found: 3
Select item for more details and to access through your institution.
A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall‐Smith Syndrome.
- Published in:
- JBMR Plus, 2023, v. 7, n. 6, p. 1, doi. 10.1002/jbm4.10739
- By:
- Publication type:
- Article
The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase.
- Published in:
- Nature Genetics, 1999, v. 22, n. 2, p. 182, doi. 10.1038/9700
- By:
- Publication type:
- Article
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type I.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 2, p. 115
- By:
- Publication type:
- Article