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

✍ Scribed by Judit Kárteszi; Katalin Hollódy; Judit Bene; Éva Morava; Kinga Hadzsiev; Márta Czakó; Béla Melegh; Alexandra Tészás; György Kosztolányi

Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
31 KB
Volume
131A
Category
Article
ISSN
1552-4825

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