Imaging in a Rare Case of Neonatal Arterial Tortuosity Syndrome.
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- Global Medical Genetics, 2023, v. 10, n. 4, p. 271, doi. 10.1055/s-0043-1775980
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Works matching IS 26999404 AND DT 2023 AND VI 10 AND IP 4
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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
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- Article