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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


Microsoft Word - mso20.doc
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Document Date: 2007-09-14 08:02:14

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File Size: 243,35 KB

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