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Rare diseases / Hypermethioninemia / Newborn screening / Medical genetics / 2-Methylbutyryl-CoA dehydrogenase deficiency / 3-Methylcrotonyl-CoA carboxylase deficiency / Medicine / Health / Genetic genealogy
Date: 2007-09-14 08:02:14
Rare diseases
Hypermethioninemia
Newborn screening
Medical genetics
2-Methylbutyryl-CoA dehydrogenase deficiency
3-Methylcrotonyl-CoA carboxylase deficiency
Medicine
Health
Genetic genealogy

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