In-frame deletion in MECP2 causes mild nonspecific mental retardation

Yntema, Helger G.; Oudakker, Astrid R.; Kleefstra, Tjitske; Hamel, Ben C. J.; van Bokhoven, Hans; Chelly, Jamel; Kalscheuer, Vera M.; Fryns, Jean-Pierre; Raynaud, Martine; Moizard, Marie-Pierre; Moraine, Claude

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In-frame deletion in MECP2 causes mild nonspecific mental retardation

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Kalscheuer, Vera M.
Chromosome Rearrangements and Disease (Vera Kalscheuer), Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Yntema, H. G., Oudakker, A. R., Kleefstra, T., Hamel, B. C. J., van Bokhoven, H., Chelly, J., Kalscheuer, V. M., Fryns, J.-P., Raynaud, M., Moizard, M.-P., & Moraine, C. (2002). In-frame deletion in MECP2 causes mild nonspecific mental retardation. American Journal of Medical Genetics, 107(1), 81-83.

引用: https://hdl.handle.net/11858/00-001M-0000-0010-8C86-0

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