Found: 4
Select item for more details and to access through your institution.
A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 19, p. 3154, doi. 10.3390/cells11193154
- By:
- Publication type:
- Article
Clinical, Radiological, and Genetic Characterization of a Patient with a Novel Homoallelic Loss-of-Function Variant in DNM1.
- Published in:
- Genes, 2022, v. 13, n. 12, p. 2252, doi. 10.3390/genes13122252
- By:
- Publication type:
- Article
Leveraging AI Advances and Online Tools for Structure‐Based Variant Analysis.
- Published in:
- Current Protocols, 2023, v. 3, n. 8, p. 1, doi. 10.1002/cpz1.857
- By:
- Publication type:
- Article
Further delineation of Wiedemann‐Rautenstrauch syndrome linked with POLR3A.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 3, p. 1, doi. 10.1002/mgg3.2274
- By:
- Publication type:
- Article