Periode | 26 feb. 2010 |
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Evenementstype | Other |
Sponsor | Belgian Society of Human Genetics |
Gerelateerde inhoud
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Onderzoeksoutput
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Molecular spectrum of androgen receptor gene alterations in Belgian patients
Onderzoeksoutput: Meeting abstract (Book)
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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C.
Onderzoeksoutput: Article › peer review
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Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to the m.14487T>C mutation in ND6.
Onderzoeksoutput: Meeting abstract (Journal)
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Progressieve myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C in ND6
Onderzoeksoutput: Meeting abstract (Book)
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Are defects in meiosis genes involved in recurrent pregnancy loss rather than in male infertility?
Onderzoeksoutput: Editorial
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Mutation analysis of the NEMO gene in patients with Incontinentia Pigmenti
Onderzoeksoutput: Meeting abstract (Book)
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