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

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

Research output: Contribution to journalLetter

3 Citations (Scopus)
Original languageEnglish (US)
Number of pages1
JournalAmerican Journal of Medical Genetics
Volume131 A
Issue number1
DOIs
StatePublished - Nov 15 2004
Externally publishedYes

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DNA Mutational Analysis
Non Histone Chromosomal Proteins
Methyl-CpG-Binding Protein 2
Repressor Proteins
Rett Syndrome
X Chromosome Inactivation
Hungary
Sequence Deletion
DNA-Binding Proteins
Missense Mutation
Mutation

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients [4]. / Kárteszi, Judit; Morava-Kozicz, Eva; Hadzsiev, Kinga; Melegh, Béla; Tészás, Alexandra; Kosztolányi, György; Hollódy, Katalin; Bene, Judit; Czakó, Márta.

In: American Journal of Medical Genetics, Vol. 131 A, No. 1, 15.11.2004.

Research output: Contribution to journalLetter

Kárteszi, Judit ; Morava-Kozicz, Eva ; Hadzsiev, Kinga ; Melegh, Béla ; Tészás, Alexandra ; Kosztolányi, György ; Hollódy, Katalin ; Bene, Judit ; Czakó, Márta. / Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients [4]. In: American Journal of Medical Genetics. 2004 ; Vol. 131 A, No. 1.
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