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

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Publication year
2004
Author(s)
Karteszi, J.
Hollody, K.
Bene, J.
Morava, E.
Hadzsiev, K.
Czako, M.
Melegh, B.
Teszas, A.
Kosztolanyi, G.Y.
Source
American Journal of Medical Genetics. Part A, 131, 1, (2004), pp. 106
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Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/58651   https://hdl.handle.net/2066/58651
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