Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome

Angela L. Duker(Children's Hospital of Michigan), Trilochan Sahoo(BioNano Genomics (United States))

European Journal of Human Genetics

June 30, 2010

10.1038/ejhg.2010.102

Cited by 320

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