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Dive into the research topics of 'Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients [4]'. Together they form a unique fingerprint.- Sort by
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Judit Kárteszi, Éva Morava, Kinga Hadzsiev, Béla Melegh, Alexandra Tészás, György Kosztolányi, Katalin Hollódy, Judit Bene, Márta Czakó
Research output: Contribution to journal › Letter › peer-review