A new case of interstitial 6q16.2 deletion in a patient with Prader–Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity
| Autor: | Varela, Monica C., Simões-Sato, Alex Y., Kim, Chong A., Bertola, Débora R., De Castro, Claudia I.E., Koiffmann, Celia P. |
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| Zdroj: | In European Journal of Medical Genetics 2006 49(4):298-305 |
| Databáze: | ScienceDirect |
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