Periode | 31 mei 2008 → 3 jun. 2008 |
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Evenementstype | Other |
Sponsor | European Society of Human Genetics |
Gerelateerde inhoud
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Onderzoeksoutput
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Infantile neuroaxonal dystrophy: challenges for identification and new advances in prenatal diagnosis.
Onderzoeksoutput: Editorial
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Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.
Onderzoeksoutput: Editorial
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projecten