Works matching IS 26999404 AND DT 2023 AND VI 10 AND IP 4
Results: 2
Imaging in a Rare Case of Neonatal Arterial Tortuosity Syndrome.
- Published in:
- Global Medical Genetics, 2023, v. 10, n. 4, p. 271, doi. 10.1055/s-0043-1775980
- By:
- Publication type:
- Article
The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13.
- Published in:
- Global Medical Genetics, 2023, v. 10, n. 4, p. 278, doi. 10.1055/s-0043-1775979
- By:
- Publication type:
- Article