9 results on '"Bracciamà, Valeria"'
Search Results
2. The role of genetic testing in the diagnostic workflow of pediatric patients with kidney diseases: the experience of a single institution
3. Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialists
4. Clinical exome sequencing is a powerful tool in the diagnostic flow of monogenic kidney diseases: an Italian experience
5. A novel COLEC10 mutation in a child with 3MC syndrome
6. Functional evaluation of a novel nonsense variant of the calcium-sensing receptor gene leading to hypocalcemia.
7. Bidirectional linkage between the B-cell receptor and NOTCH1 in chronic lymphocytic leukemia and in Richter’s syndrome: therapeutic implications
8. Correction: Bidirectional linkage between the B-cell receptor and NOTCH1 in chronic lymphocytic leukemia and in Richter’s syndrome: therapeutic implications
9. New case of syncytial giant-cell variant of hepatocellular carcinoma in a pediatric patient with HNF1B deficiency: does it fit with the syndrome?
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.