Mutations in exon 1 of MECP2B are not a common cause of X-linked mental 
retardation in males

Poirier, Karine; Francis, Fiona; Hamel, Ben; Moraine, Claude; Fryns, Jean Pierre; Ropers, Hans-Hilger; Chelly, Jamel; Bienvenu, Thierry

doi:10.1038/sj.ejhg.5201399

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Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males

Poirier, K., Francis, F., Hamel, B., Moraine, C., Fryns, J. P., Ropers, H.-H., et al. (2005). Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males. Druckausgaben (und Verfilmungen), 13(5), 523-524. doi:10.1038/sj.ejhg.5201399.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-86AF-A Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-86B0-4

Genre: Journal Article

Alternative Title : Eur J Hum Genet

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Creators:
Poirier, Karine, Author
Francis, Fiona, Author
Hamel, Ben, Author
Moraine, Claude, Author
Fryns, Jean Pierre, Author
Ropers, Hans-Hilger¹, Author
Chelly, Jamel, Author
Bienvenu, Thierry, Author

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1Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433549

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Language(s): eng - English

Dates: Date issued: 2005-03-16

Publication Status: Issued

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Identifiers: eDoc: 271565
DOI: 10.1038/sj.ejhg.5201399

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Title: Druckausgaben (und Verfilmungen)

Alternative Title : Eur J Hum Genet

Source Genre: Journal

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Pages: - Volume / Issue: 13 (5) Sequence Number: - Start / End Page: 523 - 524 Identifier: ISSN: 1018-4813