Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients [4]

Judit Kárteszi, Éva Morava, Kinga Hadzsiev, Béla Melegh, Alexandra Tészás, György Kosztolányi, Katalin Hollódy, Judit Bene, Márta Czakó

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