A novel deletion of SNURF/SNRPN exon 1 in a patient with Prader-Willi-like phenotype
| Autor: | Cao, Yang, AlHumaidi, Susan S., Faqeih, Eissa A., Pitel, Beth A., Lundquist, Patrick, Aypar, Umut |
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| Zdroj: | In European Journal of Medical Genetics August 2017 60(8):416-420 |
| Databáze: | ScienceDirect |
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