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Mutation analysis of MECP2 and determination of the X‐inactivation pattern in Hungarian Rett syndrome patients
Author(s) -
Kárteszi Judit,
Hollódy Katalin,
Bene Judit,
Morava Éva,
Hadzsiev Kinga,
Czakó Márta,
Melegh Béla,
Tészás Alexandra,
Kosztolányi György
Publication year - 2004
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.30218
Subject(s) - medical genetics , rett syndrome , medicine , genetics , pediatrics , biology , gene
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