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  In-frame deletion in MECP2 causes mild nonspecific mental retardation

Yntema, H. G., Oudakker, A. R., Kleefstra, T., Hamel, B. C. J., van Bokhoven, H., Chelly, J., et al. (2002). In-frame deletion in MECP2 causes mild nonspecific mental retardation. American Journal of Medical Genetics, 107(1), 81-83.

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 Creators:
Yntema, Helger G., Author
Oudakker, Astrid R., Author
Kleefstra, Tjitske, Author
Hamel, Ben C. J., Author
van Bokhoven, Hans, Author
Chelly, Jamel, Author
Kalscheuer, Vera M.1, Author           
Fryns, Jean-Pierre, Author
Raynaud, Martine, Author
Moizard, Marie-Pierre, Author
Moraine, Claude, Author
Affiliations:
1Chromosome Rearrangements and Disease (Vera Kalscheuer), Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479642              

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Language(s): eng - English
 Dates: 2002-01
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 24374
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Title: American Journal of Medical Genetics
Source Genre: Journal
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Pages: - Volume / Issue: 107 (1) Sequence Number: - Start / End Page: 81 - 83 Identifier: -