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

doi:10.1002/ajmg.a.30218

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

Medical Genetics

Research output: Contribution to journal › Letter › peer-review

3 Scopus citations

Original language	English (US)
Pages (from-to)	106
Number of pages	1
Journal	American Journal of Medical Genetics
Volume	131 A
Issue number	1
DOIs	https://doi.org/10.1002/ajmg.a.30218
State	Published - Nov 15 2004

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1002/ajmg.a.30218

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

author = "Judit K{\'a}rteszi and {\'E}va Morava and Kinga Hadzsiev and B{\'e}la Melegh and Alexandra T{\'e}sz{\'a}s and Gy{\"o}rgy Kosztol{\'a}nyi and Katalin Holl{\'o}dy and Judit Bene and M{\'a}rta Czak{\'o}",

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T1 - Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients [4]

AU - Kárteszi, Judit

AU - Morava, Éva

AU - Hadzsiev, Kinga

AU - Melegh, Béla

AU - Tészás, Alexandra

AU - Kosztolányi, György

AU - Hollódy, Katalin

AU - Bene, Judit

AU - Czakó, Márta

PY - 2004/11/15

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U2 - 10.1002/ajmg.a.30218

DO - 10.1002/ajmg.a.30218

M3 - Letter

C2 - 15389714

AN - SCOPUS:7244234360

SN - 1552-4825

VL - 131 A

SP - 106

JO - American Journal of Medical Genetics

JF - American Journal of Medical Genetics

IS - 1

ER -

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

ASJC Scopus subject areas

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