Associated Papers
Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
Hadzsiev K et al.
Journal of Human Genetics, 2011
Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients.
Kárteszi J et al.
American Journal of Medical Genetics. Part A, 2004
[Mutational analysis of the MECP2 gene by direct sequencing in Hungarian patients with Rett syndrome].
Kárteszi J et al.
Orvosi Hetilap, 2004
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