Familial 1.1 Mb deletion in chromosome Xq22.1 associated with mental retardation and behavioural disorders in female patients
| Autor: | Grillo, L., Reitano, S., Belfiore, G., Spalletta, A., Amata, S., Bottitta, M., Barone, C., Falco, M., Fichera, M., Romano, C. |
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| Zdroj: | In European Journal of Medical Genetics 2010 53(2):113-116 |
| Databáze: | ScienceDirect |
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